Canonical Allele Identifier: CA2361538143
Gene: PROCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176692C= , CM000682.2:g.35176692C= GRCh38
NC_000020.10:g.33764495C= , CM000682.1:g.33764495C= GRCh37
NC_000020.9:g.33228156C= NCBI36
NG_032899.1:g.9722C=
NG_032899.2:g.9722C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.602-6C= MANE Select ENSP00000216968.3:n.602-6C=
ENST00000216968.4:c.602-6C= ENSP00000216968.3:n.602-6C=
ENST00000634509.1:c.94+246C= ENSP00000489456.1:n.94+246C=
ENST00000635377.1:c.501+246C=
NM_006404.4:c.602-6C= NP_006395.2:n.602-6C=
XM_011528496.1:c.601+246C= XP_011526798.1:n.601+246C=
NM_001355008.1:c.-101-10821G= NP_001341937.1:n.-101-10821G=
NM_006404.5:c.602-6C= MANE Select NP_006395.2:n.602-6C=
NM_001355008.2:c.-101-10821G= NP_001341937.1:n.-101-10821G=