Canonical Allele Identifier: CA408710771

Gene: PROCR

Linked Data

• dbSNP Id: rs1600735516
• MyVariant Identifiers: chr20:g.33764579T>G (hg19) ; chr20:g.35176776T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176776T>G , CM000682.2:g.35176776T>G	GRCh38
NC_000020.10:g.33764579T>G , CM000682.1:g.33764579T>G	GRCh37
NC_000020.9:g.33228240T>G	NCBI36
NG_032899.1:g.9806T>G
NG_032899.2:g.9806T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.680T>G MANE Select	ENSP00000216968.3:p.Val227Gly
ENST00000216968.4:c.680T>G	ENSP00000216968.3:p.Val227Gly
ENST00000634509.1:c.94+330T>G	ENSP00000489456.1:n.94+330T>G
ENST00000635377.1:c.502-311T>G
NM_006404.4:c.680T>G	NP_006395.2:p.Val227Gly
XM_011528496.1:c.601+330T>G	XP_011526798.1:n.601+330T>G
NM_001355008.1:c.-101-10905A>C	NP_001341937.1:n.-101-10905A>C
NM_006404.5:c.680T>G MANE Select	NP_006395.2:p.Val227Gly
NM_001355008.2:c.-101-10905A>C	NP_001341937.1:n.-101-10905A>C