Canonical Allele Identifier: CA2361538147

Gene: PROCR

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176696A= , CM000682.2:g.35176696A=	GRCh38
NC_000020.10:g.33764499A= , CM000682.1:g.33764499A=	GRCh37
NC_000020.9:g.33228160A=	NCBI36
NG_032899.1:g.9726A=
NG_032899.2:g.9726A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216968.5:c.602-2A= MANE Select	ENSP00000216968.3:n.602-2A=
ENST00000216968.4:c.602-2A=	ENSP00000216968.3:n.602-2A=
ENST00000634509.1:c.94+250A=	ENSP00000489456.1:n.94+250A=
ENST00000635377.1:c.501+250A=
NM_006404.4:c.602-2A=	NP_006395.2:n.602-2A=
XM_011528496.1:c.601+250A=	XP_011526798.1:n.601+250A=
NM_001355008.1:c.-101-10825T=	NP_001341937.1:n.-101-10825T=
NM_006404.5:c.602-2A= MANE Select	NP_006395.2:n.602-2A=
NM_001355008.2:c.-101-10825T=	NP_001341937.1:n.-101-10825T=