Canonical Allele Identifier: CA1241017579

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29070896T= , CM000664.2:g.29070896T=	GRCh38
NC_000002.11:g.29293762T= , CM000664.1:g.29293762T=	GRCh37
NC_000002.10:g.29147266T=	NCBI36
NG_021427.1:g.8366A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.3366A= MANE Select	ENSP00000332809.4:p.Ile1122=
ENST00000331664.5:c.3366A=	ENSP00000332809.4:p.Ile1122=
NM_001029883.2:c.3366A=	NP_001025054.1:p.Ile1122=
XM_011532826.1:c.3366A=	XP_011531128.1:p.Ile1122=
XR_939901.1:n.185+1729T=
XR_939902.1:n.173+1741T=
NM_001029883.3:c.3366A= MANE Select	NP_001025054.1:p.Ile1122=