Canonical Allele Identifier: CA741073204
Gene: SNAP25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10239896G>C , CM000682.2:g.10239896G>C GRCh38
NC_000020.10:g.10220544G>C , CM000682.1:g.10220544G>C GRCh37
NC_000020.9:g.10168544G>C NCBI36
NG_029626.1:g.26068G>C

Transcript Alleles

HGVS Amino-acid change
NM_003081.3:c.-64+20919G>C NP_003072.2:p.=
NM_130811.2:c.-64+20919G>C NP_570824.1:p.=
XM_005260808.3:c.-64+20683G>C XP_005260865.1:p.=
XM_005260810.3:c.-64+20683G>C XP_005260867.1:p.=
NM_001322902.1:c.-64+20683G>C NP_001309831.1:p.=
NM_001322903.1:c.-64+5559G>C NP_001309832.1:p.=
NM_001322904.1:c.-64+12458G>C NP_001309833.1:p.=
NM_001322905.1:c.-123-4079G>C NP_001309834.1:p.=
NM_001322906.1:c.-64+1870G>C NP_001309835.1:p.=
NM_001322907.1:c.-64+12458G>C NP_001309836.1:p.=
NM_001322908.1:c.-241-4079G>C NP_001309837.1:p.=
NM_001322909.1:c.-108-19461G>C NP_001309838.1:p.=
NM_001322910.1:c.-64+12458G>C NP_001309839.1:p.=
NM_003081.4:c.-64+20919G>C NP_003072.2:p.=
NM_130811.3:c.-64+20919G>C NP_570824.1:p.=
XM_005260808.5:c.-64+20683G>C XP_005260865.1:p.=
XM_017028021.2:c.-123-4079G>C XP_016883510.1:p.=
XM_017028022.1:c.-64+1870G>C XP_016883511.1:p.=
NM_001322902.2:c.-64+20683G>C NP_001309831.1:p.=
NM_001322903.2:c.-64+5559G>C NP_001309832.1:p.=
NM_001322904.2:c.-64+12458G>C NP_001309833.1:p.=
NM_001322905.2:c.-123-4079G>C NP_001309834.1:p.=
NM_001322906.2:c.-64+1870G>C NP_001309835.1:p.=
NM_001322907.2:c.-64+12458G>C NP_001309836.1:p.=
NM_001322908.2:c.-241-4079G>C NP_001309837.1:p.=
NM_001322909.2:c.-108-19461G>C NP_001309838.1:p.=
NM_001322910.2:c.-64+12458G>C NP_001309839.1:p.=
NM_003081.5:c.-64+20919G>C NP_003072.2:p.=
NM_130811.4:c.-64+20919G>C MANE Select NP_570824.1:p.=
ENST00000254976.6:c.-64+20919G>C ENSP00000254976.2:p.=
ENST00000304886.6:c.-64+20919G>C ENSP00000307341.2:p.=
ENST00000430336.1:c.-64+20683G>C ENSP00000400720.1:p.=