Canonical Allele Identifier: CA2361537828

Gene: PROCR

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176012G= , CM000682.2:g.35176012G=	GRCh38
NC_000020.10:g.33763815G= , CM000682.1:g.33763815G=	GRCh37
NC_000020.9:g.33227476G=	NCBI36
NG_032899.1:g.9042G=
NG_032899.2:g.9042G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-156G= MANE Select	ENSP00000216968.3:n.323-156G=
ENST00000216968.4:c.323-156G=	ENSP00000216968.3:n.323-156G=
ENST00000635377.1:c.223-156G=
NM_006404.4:c.323-156G=	NP_006395.2:n.323-156G=
XM_011528496.1:c.323-156G=	XP_011526798.1:n.323-156G=
NM_001355008.1:c.-101-10141C=	NP_001341937.1:n.-101-10141C=
NM_006404.5:c.323-156G= MANE Select	NP_006395.2:n.323-156G=
NM_001355008.2:c.-101-10141C=	NP_001341937.1:n.-101-10141C=