Canonical Allele Identifier: CA2577380333

Gene: PROCR

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35176078C>A , CM000682.2:g.35176078C>A	GRCh38
NC_000020.10:g.33763881C>A , CM000682.1:g.33763881C>A	GRCh37
NC_000020.9:g.33227542C>A	NCBI36
NG_032899.1:g.9108C>A
NG_032899.2:g.9108C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216968.5:c.323-90C>A MANE Select	ENSP00000216968.3:n.323-90C>A
ENST00000216968.4:c.323-90C>A	ENSP00000216968.3:n.323-90C>A
ENST00000635377.1:c.223-90C>A
NM_006404.4:c.323-90C>A	NP_006395.2:n.323-90C>A
XM_011528496.1:c.323-90C>A	XP_011526798.1:n.323-90C>A
NM_001355008.1:c.-101-10207G>T	NP_001341937.1:n.-101-10207G>T
NM_006404.5:c.323-90C>A MANE Select	NP_006395.2:n.323-90C>A
NM_001355008.2:c.-101-10207G>T	NP_001341937.1:n.-101-10207G>T