Canonical Allele Identifier: CA2360752994

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438672C= , CM000682.2:g.33438672C=	GRCh38
NC_000020.10:g.32026478C= , CM000682.1:g.32026478C=	GRCh37
NC_000020.9:g.31490139C=	NCBI36
NG_011622.1:g.10221G= , LRG_332:g.10221G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+169G= MANE Select	ENSP00000217381.2:n.496+169G=
ENST00000217381.2:c.496+169G=	ENSP00000217381.2:n.496+169G=
NM_003098.2:c.496+169G= , LRG_332t1:c.496+169G=	NP_003089.1:n.496+169G=
XM_005260517.1:c.496+169G=	XP_005260574.1:n.496+169G=
XM_011529007.1:c.496+169G=	XP_011527309.1:n.496+169G=
XM_011529008.1:c.496+169G=	XP_011527310.1:n.496+169G=
XR_936612.1:n.729+169G=
XM_024451971.1:c.169+169G=	XP_024307739.1:n.169+169G=
NM_003098.3:c.496+169G= MANE Select	NP_003089.1:n.496+169G=