Canonical Allele Identifier: CA408710666
Gene: PROCR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176754T>A , CM000682.2:g.35176754T>A GRCh38
NC_000020.10:g.33764557T>A , CM000682.1:g.33764557T>A GRCh37
NC_000020.9:g.33228218T>A NCBI36
NG_032899.1:g.9784T>A
NG_032899.2:g.9784T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000216968.5:c.658T>A MANE Select ENSP00000216968.3:p.Phe220Ile
ENST00000216968.4:c.658T>A ENSP00000216968.3:p.Phe220Ile
ENST00000634509.1:c.94+308T>A ENSP00000489456.1:n.94+308T>A
ENST00000635377.1:c.501+308T>A
NM_006404.4:c.658T>A NP_006395.2:p.Phe220Ile
XM_011528496.1:c.601+308T>A XP_011526798.1:n.601+308T>A
NM_001355008.1:c.-101-10883A>T NP_001341937.1:n.-101-10883A>T
NM_006404.5:c.658T>A MANE Select NP_006395.2:p.Phe220Ile
NM_001355008.2:c.-101-10883A>T NP_001341937.1:n.-101-10883A>T