Canonical Allele Identifier: CA425437965

Gene: PCARE

Linked Data

• MyVariant Identifiers: chr2:g.29293507G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29070641G>T , CM000664.2:g.29070641G>T	GRCh38
NC_000002.11:g.29293507G>T , CM000664.1:g.29293507G>T	GRCh37
NC_000002.10:g.29147011G>T	NCBI36
NG_021427.1:g.8621C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3621C>A MANE Select	ENSP00000332809.4:p.Thr1207=
ENST00000331664.5:c.3621C>A	ENSP00000332809.4:p.Thr1207=
NM_001029883.2:c.3621C>A	NP_001025054.1:p.Thr1207=
XM_011532826.1:c.3621C>A	XP_011531128.1:p.Thr1207=
XR_939901.1:n.185+1474G>T
XR_939902.1:n.173+1486G>T
NM_001029883.3:c.3621C>A MANE Select	NP_001025054.1:p.Thr1207=