Canonical Allele Identifier: CA44643305

Gene: PCARE

Linked Data

• dbSNP Id: rs368965009
• MyVariant Identifiers: chr2:g.29296007G>A (hg19) ; chr2:g.29073141G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073141G>A , CM000664.2:g.29073141G>A	GRCh38
NC_000002.11:g.29296007G>A , CM000664.1:g.29296007G>A	GRCh37
NC_000002.10:g.29149511G>A	NCBI36
NG_021427.1:g.6121C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1121C>T MANE Select	ENSP00000332809.4:p.Ala374Val
ENST00000331664.5:c.1121C>T	ENSP00000332809.4:p.Ala374Val
NM_001029883.2:c.1121C>T	NP_001025054.1:p.Ala374Val
XM_011532826.1:c.1121C>T	XP_011531128.1:p.Ala374Val
XR_939901.1:n.185+3974G>A
XR_939902.1:n.173+3986G>A
NM_001029883.3:c.1121C>T MANE Select	NP_001025054.1:p.Ala374Val