Canonical Allele Identifier: CA425617678

Gene: PCARE

Linked Data

• gnomAD v4: 2-29072876-C-A
• MyVariant Identifiers: chr2:g.29295742C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29072876C>A , CM000664.2:g.29072876C>A	GRCh38
NC_000002.11:g.29295742C>A , CM000664.1:g.29295742C>A	GRCh37
NC_000002.10:g.29149246C>A	NCBI36
NG_021427.1:g.6386G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1386G>T MANE Select	ENSP00000332809.4:p.Gly462=
ENST00000331664.5:c.1386G>T	ENSP00000332809.4:p.Gly462=
NM_001029883.2:c.1386G>T	NP_001025054.1:p.Gly462=
XM_011532826.1:c.1386G>T	XP_011531128.1:p.Gly462=
XR_939901.1:n.185+3709C>A
XR_939902.1:n.173+3721C>A
NM_001029883.3:c.1386G>T MANE Select	NP_001025054.1:p.Gly462=