Canonical Allele Identifier: CA2816230980
Gene: PROCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35175725C>A , CM000682.2:g.35175725C>A GRCh38
NC_000020.10:g.33763528C>A , CM000682.1:g.33763528C>A GRCh37
NC_000020.9:g.33227189C>A NCBI36
NG_032899.1:g.8755C>A
NG_032899.2:g.8755C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.323-443C>A MANE Select ENSP00000216968.3:n.323-443C>A
ENST00000216968.4:c.323-443C>A ENSP00000216968.3:n.323-443C>A
ENST00000635377.1:c.223-443C>A
NM_006404.4:c.323-443C>A NP_006395.2:n.323-443C>A
XM_011528496.1:c.323-443C>A XP_011526798.1:n.323-443C>A
NM_001355008.1:c.-101-9854G>T NP_001341937.1:n.-101-9854G>T
NM_006404.5:c.323-443C>A MANE Select NP_006395.2:n.323-443C>A
NM_001355008.2:c.-101-9854G>T NP_001341937.1:n.-101-9854G>T
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