Canonical Allele Identifier: CA2360752964

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438599G= , CM000682.2:g.33438599G=	GRCh38
NC_000020.10:g.32026405G= , CM000682.1:g.32026405G=	GRCh37
NC_000020.9:g.31490066G=	NCBI36
NG_011622.1:g.10294C= , LRG_332:g.10294C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+242C= MANE Select	ENSP00000217381.2:n.496+242C=
ENST00000217381.2:c.496+242C=	ENSP00000217381.2:n.496+242C=
NM_003098.2:c.496+242C= , LRG_332t1:c.496+242C=	NP_003089.1:n.496+242C=
XM_005260517.1:c.496+242C=	XP_005260574.1:n.496+242C=
XM_011529007.1:c.496+242C=	XP_011527309.1:n.496+242C=
XM_011529008.1:c.496+242C=	XP_011527310.1:n.496+242C=
XR_936612.1:n.729+242C=
XM_024451971.1:c.169+242C=	XP_024307739.1:n.169+242C=
NM_003098.3:c.496+242C= MANE Select	NP_003089.1:n.496+242C=