Canonical Allele Identifier: CA408710481

Gene: PROCR

Linked Data

• gnomAD v4: 20-35176698-G-A
• MyVariant Identifiers: chr20:g.33764501G>A (hg19) ; chr20:g.35176698G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176698G>A , CM000682.2:g.35176698G>A	GRCh38
NC_000020.10:g.33764501G>A , CM000682.1:g.33764501G>A	GRCh37
NC_000020.9:g.33228162G>A	NCBI36
NG_032899.1:g.9728G>A
NG_032899.2:g.9728G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216968.5:c.602G>A MANE Select	ENSP00000216968.3:p.Gly201Glu
ENST00000216968.4:c.602G>A	ENSP00000216968.3:p.Gly201Glu
ENST00000634509.1:c.94+252G>A	ENSP00000489456.1:n.94+252G>A
ENST00000635377.1:c.501+252G>A
NM_006404.4:c.602G>A	NP_006395.2:p.Gly201Glu
XM_011528496.1:c.601+252G>A	XP_011526798.1:n.601+252G>A
NM_001355008.1:c.-101-10827C>T	NP_001341937.1:n.-101-10827C>T
NM_006404.5:c.602G>A MANE Select	NP_006395.2:p.Gly201Glu
NM_001355008.2:c.-101-10827C>T	NP_001341937.1:n.-101-10827C>T