Canonical Allele Identifier: CA408710656
Gene: PROCR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176751A>C , CM000682.2:g.35176751A>C GRCh38
NC_000020.10:g.33764554A>C , CM000682.1:g.33764554A>C GRCh37
NC_000020.9:g.33228215A>C NCBI36
NG_032899.1:g.9781A>C
NG_032899.2:g.9781A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000216968.5:c.655A>C MANE Select ENSP00000216968.3:p.Ser219Arg
ENST00000216968.4:c.655A>C ENSP00000216968.3:p.Ser219Arg
ENST00000634509.1:c.94+305A>C ENSP00000489456.1:n.94+305A>C
ENST00000635377.1:c.501+305A>C
NM_006404.4:c.655A>C NP_006395.2:p.Ser219Arg
XM_011528496.1:c.601+305A>C XP_011526798.1:n.601+305A>C
NM_001355008.1:c.-101-10880T>G NP_001341937.1:n.-101-10880T>G
NM_006404.5:c.655A>C MANE Select NP_006395.2:p.Ser219Arg
NM_001355008.2:c.-101-10880T>G NP_001341937.1:n.-101-10880T>G