Canonical Allele Identifier: CA2349705206
Gene: SNAP25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10239771_10239772delinsTG , CM000682.2:g.10239771_10239772delinsTG GRCh38
NC_000020.10:g.10220419_10220420delinsTG , CM000682.1:g.10220419_10220420delinsTG GRCh37
NC_000020.9:g.10168419_10168420delinsTG NCBI36
NG_029626.1:g.25943_25944delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000706269.1:c.-64+20558_-64+20559delinsTG ENSP00000516314.1:n.-64+20558_-64+20559de...
ENST00000685131.1:c.-64+1745_-64+1746delinsTG ENSP00000508837.1:n.-64+1745_-64+1746deli...
ENST00000687785.1:c.-241-4204_-241-4203delinsTG ENSP00000510219.1:n.-241-4204_-241-4203de...
ENST00000689077.1:n.393-35658_393-35657delinsTG
ENST00000689248.1:n.97-4981_97-4980delinsTG
ENST00000689757.1:c.-109+12333_-109+12334delinsTG ENSP00000509312.1:n.-109+12333_-109+12334...
ENST00000689858.1:c.-123-4204_-123-4203delinsTG ENSP00000510663.1:n.-123-4204_-123-4203de...
ENST00000690099.1:n.393-35658_393-35657delinsTG
ENST00000690766.1:n.393-35658_393-35657delinsTG
ENST00000690812.1:c.-168-4204_-168-4203delinsTG ENSP00000509287.1:n.-168-4204_-168-4203de...
ENST00000691161.1:c.-64+12333_-64+12334delinsTG ENSP00000510109.1:n.-64+12333_-64+12334de...
ENST00000691353.1:c.-263+20558_-263+20559delinsTG ENSP00000509759.1:n.-263+20558_-263+20559...
ENST00000691665.1:c.-64+5434_-64+5435delinsTG ENSP00000508541.1:n.-64+5434_-64+5435deli...
ENST00000692411.1:c.-149+20794_-149+20795delinsTG ENSP00000508939.1:n.-149+20794_-149+20795...
ENST00000693325.1:c.-64+12333_-64+12334delinsTG ENSP00000510558.1:n.-64+12333_-64+12334de...
ENST00000693732.1:n.393-35658_393-35657delinsTG
ENST00000254976.7:c.-64+20794_-64+20795delinsTG MANE Select ENSP00000254976.3:n.-64+20794_-64+20795de...
ENST00000254976.6:c.-64+20794_-64+20795delinsTG ENSP00000254976.2:n.-64+20794_-64+20795de...
ENST00000304886.6:c.-64+20794_-64+20795delinsTG ENSP00000307341.2:n.-64+20794_-64+20795de...
ENST00000430336.1:c.-64+20558_-64+20559delinsTG ENSP00000400720.1:n.-64+20558_-64+20559de...
NM_003081.3:c.-64+20794_-64+20795delinsTG NP_003072.2:n.-64+20794_-64+20795delinsTG...
NM_130811.2:c.-64+20794_-64+20795delinsTG NP_570824.1:n.-64+20794_-64+20795delinsTG...
XM_005260808.3:c.-64+20558_-64+20559delinsTG XP_005260865.1:n.-64+20558_-64+20559delin...
XM_005260810.3:c.-64+20558_-64+20559delinsTG XP_005260867.1:n.-64+20558_-64+20559delin...
NM_001322902.1:c.-64+20558_-64+20559delinsTG NP_001309831.1:n.-64+20558_-64+20559delin...
NM_001322903.1:c.-64+5434_-64+5435delinsTG NP_001309832.1:n.-64+5434_-64+5435delinsT...
NM_001322904.1:c.-64+12333_-64+12334delinsTG NP_001309833.1:n.-64+12333_-64+12334delin...
NM_001322905.1:c.-123-4204_-123-4203delinsTG NP_001309834.1:n.-123-4204_-123-4203delin...
NM_001322906.1:c.-64+1745_-64+1746delinsTG NP_001309835.1:n.-64+1745_-64+1746delinsT...
NM_001322907.1:c.-64+12333_-64+12334delinsTG NP_001309836.1:n.-64+12333_-64+12334delin...
NM_001322908.1:c.-241-4204_-241-4203delinsTG NP_001309837.1:n.-241-4204_-241-4203delin...
NM_001322909.1:c.-108-19586_-108-19585delinsTG NP_001309838.1:n.-108-19586_-108-19585del...
NM_001322910.1:c.-64+12333_-64+12334delinsTG NP_001309839.1:n.-64+12333_-64+12334delin...
NM_003081.4:c.-64+20794_-64+20795delinsTG NP_003072.2:n.-64+20794_-64+20795delinsTG...
NM_130811.3:c.-64+20794_-64+20795delinsTG NP_570824.1:n.-64+20794_-64+20795delinsTG...
XM_005260808.5:c.-64+20558_-64+20559delinsTG XP_005260865.1:n.-64+20558_-64+20559delin...
XM_017028021.2:c.-123-4204_-123-4203delinsTG XP_016883510.1:n.-123-4204_-123-4203delin...
XM_017028022.1:c.-64+1745_-64+1746delinsTG XP_016883511.1:n.-64+1745_-64+1746delinsT...
NM_001322902.2:c.-64+20558_-64+20559delinsTG NP_001309831.1:n.-64+20558_-64+20559delin...
NM_001322903.2:c.-64+5434_-64+5435delinsTG NP_001309832.1:n.-64+5434_-64+5435delinsT...
NM_001322904.2:c.-64+12333_-64+12334delinsTG NP_001309833.1:n.-64+12333_-64+12334delin...
NM_001322905.2:c.-123-4204_-123-4203delinsTG NP_001309834.1:n.-123-4204_-123-4203delin...
NM_001322906.2:c.-64+1745_-64+1746delinsTG NP_001309835.1:n.-64+1745_-64+1746delinsT...
NM_001322907.2:c.-64+12333_-64+12334delinsTG NP_001309836.1:n.-64+12333_-64+12334delin...
NM_001322908.2:c.-241-4204_-241-4203delinsTG NP_001309837.1:n.-241-4204_-241-4203delin...
NM_001322909.2:c.-108-19586_-108-19585delinsTG NP_001309838.1:n.-108-19586_-108-19585del...
NM_001322910.2:c.-64+12333_-64+12334delinsTG NP_001309839.1:n.-64+12333_-64+12334delin...
NM_003081.5:c.-64+20794_-64+20795delinsTG NP_003072.2:n.-64+20794_-64+20795delinsTG...
NM_130811.4:c.-64+20794_-64+20795delinsTG MANE Select NP_570824.1:n.-64+20794_-64+20795delinsTG...