Canonical Allele Identifier: CA408710773

Gene: PROCR

Linked Data

• MyVariant Identifiers: chr20:g.33764581G>A (hg19) ; chr20:g.35176778G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176778G>A , CM000682.2:g.35176778G>A	GRCh38
NC_000020.10:g.33764581G>A , CM000682.1:g.33764581G>A	GRCh37
NC_000020.9:g.33228242G>A	NCBI36
NG_032899.1:g.9808G>A
NG_032899.2:g.9808G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.682G>A MANE Select	ENSP00000216968.3:p.Gly228Ser
ENST00000216968.4:c.682G>A	ENSP00000216968.3:p.Gly228Ser
ENST00000634509.1:c.94+332G>A	ENSP00000489456.1:n.94+332G>A
ENST00000635377.1:c.502-309G>A
NM_006404.4:c.682G>A	NP_006395.2:p.Gly228Ser
XM_011528496.1:c.601+332G>A	XP_011526798.1:n.601+332G>A
NM_001355008.1:c.-101-10907C>T	NP_001341937.1:n.-101-10907C>T
NM_006404.5:c.682G>A MANE Select	NP_006395.2:p.Gly228Ser
NM_001355008.2:c.-101-10907C>T	NP_001341937.1:n.-101-10907C>T