Canonical Allele Identifier: CA2361538180
Community Standard Title: NM_006404.5(PROCR):c.655A= (p.Ser219=)
Gene: PROCR HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_006404.5:c.655A= MANE Select NP_006395.2:p.Ser219=
ENST00000216968.5:c.655A= MANE Select ENSP00000216968.3:p.Ser219=
NM_001355008.1:c.-101-10880T= NP_001341937.1:n.-101-10880T=
NM_001355008.2:c.-101-10880T= NP_001341937.1:n.-101-10880T=
NM_006404.4:c.655A= NP_006395.2:p.Ser219=
ENST00000216968.4:c.655A= ENSP00000216968.3:p.Ser219=
ENST00000634509.1:c.94+305A= ENSP00000489456.1:n.94+305A=
ENST00000635377.1:c.501+305A=
XM_011528496.1:c.601+305A= XP_011526798.1:n.601+305A=