Canonical Allele Identifier: CA741073195
Gene: SNAP25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10239878C>T , CM000682.2:g.10239878C>T GRCh38
NC_000020.10:g.10220526C>T , CM000682.1:g.10220526C>T GRCh37
NC_000020.9:g.10168526C>T NCBI36
NG_029626.1:g.26050C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000254976.7:c.-64+20901C>T MANE Select ENSP00000254976.3:p.=
ENST00000254976.6:c.-64+20901C>T ENSP00000254976.2:p.=
ENST00000304886.6:c.-64+20901C>T ENSP00000307341.2:p.=
ENST00000430336.1:c.-64+20665C>T ENSP00000400720.1:p.=
NM_003081.3:c.-64+20901C>T NP_003072.2:p.=
NM_130811.2:c.-64+20901C>T NP_570824.1:p.=
XM_005260808.3:c.-64+20665C>T XP_005260865.1:p.=
XM_005260810.3:c.-64+20665C>T XP_005260867.1:p.=
NM_001322902.1:c.-64+20665C>T NP_001309831.1:p.=
NM_001322903.1:c.-64+5541C>T NP_001309832.1:p.=
NM_001322904.1:c.-64+12440C>T NP_001309833.1:p.=
NM_001322905.1:c.-123-4097C>T NP_001309834.1:p.=
NM_001322906.1:c.-64+1852C>T NP_001309835.1:p.=
NM_001322907.1:c.-64+12440C>T NP_001309836.1:p.=
NM_001322908.1:c.-241-4097C>T NP_001309837.1:p.=
NM_001322909.1:c.-108-19479C>T NP_001309838.1:p.=
NM_001322910.1:c.-64+12440C>T NP_001309839.1:p.=
NM_003081.4:c.-64+20901C>T NP_003072.2:p.=
NM_130811.3:c.-64+20901C>T NP_570824.1:p.=
XM_005260808.5:c.-64+20665C>T XP_005260865.1:p.=
XM_017028021.2:c.-123-4097C>T XP_016883510.1:p.=
XM_017028022.1:c.-64+1852C>T XP_016883511.1:p.=
NM_001322902.2:c.-64+20665C>T NP_001309831.1:p.=
NM_001322903.2:c.-64+5541C>T NP_001309832.1:p.=
NM_001322904.2:c.-64+12440C>T NP_001309833.1:p.=
NM_001322905.2:c.-123-4097C>T NP_001309834.1:p.=
NM_001322906.2:c.-64+1852C>T NP_001309835.1:p.=
NM_001322907.2:c.-64+12440C>T NP_001309836.1:p.=
NM_001322908.2:c.-241-4097C>T NP_001309837.1:p.=
NM_001322909.2:c.-108-19479C>T NP_001309838.1:p.=
NM_001322910.2:c.-64+12440C>T NP_001309839.1:p.=
NM_003081.5:c.-64+20901C>T NP_003072.2:p.=
NM_130811.4:c.-64+20901C>T MANE Select NP_570824.1:p.=