Canonical Allele Identifier: CA510296775

Gene: PROCR

Linked Data

• MyVariant Identifiers: chr20:g.33764580A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176777A>T , CM000682.2:g.35176777A>T	GRCh38
NC_000020.10:g.33764580A>T , CM000682.1:g.33764580A>T	GRCh37
NC_000020.9:g.33228241A>T	NCBI36
NG_032899.1:g.9807A>T
NG_032899.2:g.9807A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.681A>T MANE Select	ENSP00000216968.3:p.Val227=
ENST00000216968.4:c.681A>T	ENSP00000216968.3:p.Val227=
ENST00000634509.1:c.94+331A>T	ENSP00000489456.1:n.94+331A>T
ENST00000635377.1:c.502-310A>T
NM_006404.4:c.681A>T	NP_006395.2:p.Val227=
XM_011528496.1:c.601+331A>T	XP_011526798.1:n.601+331A>T
NM_001355008.1:c.-101-10906T>A	NP_001341937.1:n.-101-10906T>A
NM_006404.5:c.681A>T MANE Select	NP_006395.2:p.Val227=
NM_001355008.2:c.-101-10906T>A	NP_001341937.1:n.-101-10906T>A