Canonical Allele Identifier: CA425618095

Gene: PCARE

Linked Data

• MyVariant Identifiers: chr2:g.29296495G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073629G>T , CM000664.2:g.29073629G>T	GRCh38
NC_000002.11:g.29296495G>T , CM000664.1:g.29296495G>T	GRCh37
NC_000002.10:g.29149999G>T	NCBI36
NG_021427.1:g.5633C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.633C>A MANE Select	ENSP00000332809.4:p.Thr211=
ENST00000331664.5:c.633C>A	ENSP00000332809.4:p.Thr211=
NM_001029883.2:c.633C>A	NP_001025054.1:p.Thr211=
XM_011532826.1:c.633C>A	XP_011531128.1:p.Thr211=
XR_939901.1:n.185+4462G>T
XR_939902.1:n.173+4474G>T
NM_001029883.3:c.633C>A MANE Select	NP_001025054.1:p.Thr211=