Canonical Allele Identifier: CA2361538190

Gene: PROCR

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176775G= , CM000682.2:g.35176775G=	GRCh38
NC_000020.10:g.33764578G= , CM000682.1:g.33764578G=	GRCh37
NC_000020.9:g.33228239G=	NCBI36
NG_032899.1:g.9805G=
NG_032899.2:g.9805G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.679G= MANE Select	ENSP00000216968.3:p.Val227=
ENST00000216968.4:c.679G=	ENSP00000216968.3:p.Val227=
ENST00000634509.1:c.94+329G=	ENSP00000489456.1:n.94+329G=
ENST00000635377.1:c.502-312G=
NM_006404.4:c.679G=	NP_006395.2:p.Val227=
XM_011528496.1:c.601+329G=	XP_011526798.1:n.601+329G=
NM_001355008.1:c.-101-10904C=	NP_001341937.1:n.-101-10904C=
NM_006404.5:c.679G= MANE Select	NP_006395.2:p.Val227=
NM_001355008.2:c.-101-10904C=	NP_001341937.1:n.-101-10904C=