Canonical Allele Identifier: CA425617752

Gene: PCARE

Linked Data

• MyVariant Identifiers: chr2:g.29296003T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073137T>A , CM000664.2:g.29073137T>A	GRCh38
NC_000002.11:g.29296003T>A , CM000664.1:g.29296003T>A	GRCh37
NC_000002.10:g.29149507T>A	NCBI36
NG_021427.1:g.6125A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1125A>T MANE Select	ENSP00000332809.4:p.Pro375=
ENST00000331664.5:c.1125A>T	ENSP00000332809.4:p.Pro375=
NM_001029883.2:c.1125A>T	NP_001025054.1:p.Pro375=
XM_011532826.1:c.1125A>T	XP_011531128.1:p.Pro375=
XR_939901.1:n.185+3970T>A
XR_939902.1:n.173+3982T>A
NM_001029883.3:c.1125A>T MANE Select	NP_001025054.1:p.Pro375=