Canonical Allele Identifier: CA354153082

Gene: CSTA

Linked Data

• MyVariant Identifiers: chr3:g.122060293C>A (hg19) ; chr3:g.122341446C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122341446C>A , CM000665.2:g.122341446C>A	GRCh38
NC_000003.11:g.122060293C>A , CM000665.1:g.122060293C>A	GRCh37
NC_000003.10:g.123542983C>A	NCBI36
NG_027995.1:g.21283C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264474.4:c.176C>A MANE Select	ENSP00000264474.3:p.Ala59Glu
ENST00000264474.3:c.176C>A	ENSP00000264474.3:p.Ala59Glu
NM_005213.3:c.176C>A	NP_005204.1:p.Ala59Glu
NM_005213.4:c.176C>A MANE Select	NP_005204.1:p.Ala59Glu