Canonical Allele Identifier: CA1015342121
Gene: SNAP25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10239859C>T , CM000682.2:g.10239859C>T GRCh38
NC_000020.10:g.10220507C>T , CM000682.1:g.10220507C>T GRCh37
NC_000020.9:g.10168507C>T NCBI36
NG_029626.1:g.26031C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000254976.7:c.-64+20882C>T MANE Select ENSP00000254976.3:p.=
ENST00000254976.6:c.-64+20882C>T ENSP00000254976.2:p.=
ENST00000304886.6:c.-64+20882C>T ENSP00000307341.2:p.=
ENST00000430336.1:c.-64+20646C>T ENSP00000400720.1:p.=
NM_003081.3:c.-64+20882C>T NP_003072.2:p.=
NM_130811.2:c.-64+20882C>T NP_570824.1:p.=
XM_005260808.3:c.-64+20646C>T XP_005260865.1:p.=
XM_005260810.3:c.-64+20646C>T XP_005260867.1:p.=
NM_001322902.1:c.-64+20646C>T NP_001309831.1:p.=
NM_001322903.1:c.-64+5522C>T NP_001309832.1:p.=
NM_001322904.1:c.-64+12421C>T NP_001309833.1:p.=
NM_001322905.1:c.-123-4116C>T NP_001309834.1:p.=
NM_001322906.1:c.-64+1833C>T NP_001309835.1:p.=
NM_001322907.1:c.-64+12421C>T NP_001309836.1:p.=
NM_001322908.1:c.-241-4116C>T NP_001309837.1:p.=
NM_001322909.1:c.-108-19498C>T NP_001309838.1:p.=
NM_001322910.1:c.-64+12421C>T NP_001309839.1:p.=
NM_003081.4:c.-64+20882C>T NP_003072.2:p.=
NM_130811.3:c.-64+20882C>T NP_570824.1:p.=
XM_005260808.5:c.-64+20646C>T XP_005260865.1:p.=
XM_017028021.2:c.-123-4116C>T XP_016883510.1:p.=
XM_017028022.1:c.-64+1833C>T XP_016883511.1:p.=
NM_001322902.2:c.-64+20646C>T NP_001309831.1:p.=
NM_001322903.2:c.-64+5522C>T NP_001309832.1:p.=
NM_001322904.2:c.-64+12421C>T NP_001309833.1:p.=
NM_001322905.2:c.-123-4116C>T NP_001309834.1:p.=
NM_001322906.2:c.-64+1833C>T NP_001309835.1:p.=
NM_001322907.2:c.-64+12421C>T NP_001309836.1:p.=
NM_001322908.2:c.-241-4116C>T NP_001309837.1:p.=
NM_001322909.2:c.-108-19498C>T NP_001309838.1:p.=
NM_001322910.2:c.-64+12421C>T NP_001309839.1:p.=
NM_003081.5:c.-64+20882C>T NP_003072.2:p.=
NM_130811.4:c.-64+20882C>T MANE Select NP_570824.1:p.=