Canonical Allele Identifier: CA1241013465

Gene: PCARE

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29073147T= , CM000664.2:g.29073147T=	GRCh38
NC_000002.11:g.29296013T= , CM000664.1:g.29296013T=	GRCh37
NC_000002.10:g.29149517T=	NCBI36
NG_021427.1:g.6115A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331664.6:c.1115A= MANE Select	ENSP00000332809.4:p.Asp372=
ENST00000331664.5:c.1115A=	ENSP00000332809.4:p.Asp372=
NM_001029883.2:c.1115A=	NP_001025054.1:p.Asp372=
XM_011532826.1:c.1115A=	XP_011531128.1:p.Asp372=
XR_939901.1:n.185+3980T=
XR_939902.1:n.173+3992T=
NM_001029883.3:c.1115A= MANE Select	NP_001025054.1:p.Asp372=