Canonical Allele Identifier: CA510296736

Gene: PROCR

Linked Data

• MyVariant Identifiers: chr20:g.33764574G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176771G>T , CM000682.2:g.35176771G>T	GRCh38
NC_000020.10:g.33764574G>T , CM000682.1:g.33764574G>T	GRCh37
NC_000020.9:g.33228235G>T	NCBI36
NG_032899.1:g.9801G>T
NG_032899.2:g.9801G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.675G>T MANE Select	ENSP00000216968.3:p.Val225=
ENST00000216968.4:c.675G>T	ENSP00000216968.3:p.Val225=
ENST00000634509.1:c.94+325G>T	ENSP00000489456.1:n.94+325G>T
ENST00000635377.1:c.502-316G>T
NM_006404.4:c.675G>T	NP_006395.2:p.Val225=
XM_011528496.1:c.601+325G>T	XP_011526798.1:n.601+325G>T
NM_001355008.1:c.-101-10900C>A	NP_001341937.1:n.-101-10900C>A
NM_006404.5:c.675G>T MANE Select	NP_006395.2:p.Val225=
NM_001355008.2:c.-101-10900C>A	NP_001341937.1:n.-101-10900C>A