Canonical Allele Identifier: CA1717178134

Gene: STX1A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73707017A= , CM000669.2:g.73707017A=	GRCh38
NC_000007.13:g.73121347A= , CM000669.1:g.73121347A=	GRCh37
NC_000007.12:g.72759283A=	NCBI36
NG_013360.1:g.17671T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222812.8:c.208+1572T= MANE Select	ENSP00000222812.3:n.208+1572T=
ENST00000222812.7:c.208+1572T=	ENSP00000222812.3:n.208+1572T=
ENST00000395154.7:c.208+1572T=	ENSP00000378583.3:n.208+1572T=
ENST00000395155.3:c.208+1572T=	ENSP00000378584.3:n.208+1572T=
ENST00000395156.7:c.208+1572T=	ENSP00000378585.3:n.208+1572T=
ENST00000462135.1:n.249+1572T=
ENST00000470878.5:n.357+1572T=
NM_001165903.1:c.208+1572T=	NP_001159375.1:n.208+1572T=
NM_004603.3:c.208+1572T=	NP_004594.1:n.208+1572T=
XM_011516541.1:c.121+1572T=	XP_011514843.1:n.121+1572T=
XR_242263.1:n.279+1572T=
XR_927527.1:n.279+1572T=
XR_927528.1:n.332+1572T=
XM_017012567.2:c.208+1572T=	XP_016868056.1:n.208+1572T=
XR_242263.2:n.250+1572T=
XR_927527.2:n.250+1572T=
NM_004603.4:c.208+1572T= MANE Select	NP_004594.1:n.208+1572T=
NM_001165903.2:c.208+1572T=	NP_001159375.1:n.208+1572T=