Canonical Allele Identifier: CA9830385
Gene: PROCR HGNC NCBI

Linked Data

dbSNP Id: rs9574

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176829C>G , CM000682.2:g.35176829C>G GRCh38
NC_000020.10:g.33764632C>G , CM000682.1:g.33764632C>G GRCh37
NC_000020.9:g.33228293C>G NCBI36
NG_032899.1:g.9859C>G
NG_032899.2:g.9859C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000216968.5:c.*16C>G MANE Select ENSP00000216968.3:n.*16C>G
ENST00000216968.4:c.*16C>G ENSP00000216968.3:n.*16C>G
ENST00000634509.1:c.94+383C>G ENSP00000489456.1:n.94+383C>G
ENST00000635377.1:c.502-258C>G
NM_006404.4:c.*16C>G NP_006395.2:n.*16C>G
XM_011528496.1:c.601+383C>G XP_011526798.1:n.601+383C>G
NM_001355008.1:c.-101-10958G>C NP_001341937.1:n.-101-10958G>C
NM_006404.5:c.*16C>G MANE Select NP_006395.2:n.*16C>G
NM_001355008.2:c.-101-10958G>C NP_001341937.1:n.-101-10958G>C