Canonical Allele Identifier: CA2361537782
Gene: PROCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35175912A= , CM000682.2:g.35175912A= GRCh38
NC_000020.10:g.33763715A= , CM000682.1:g.33763715A= GRCh37
NC_000020.9:g.33227376A= NCBI36
NG_032899.1:g.8942A=
NG_032899.2:g.8942A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.323-256A= MANE Select ENSP00000216968.3:n.323-256A=
ENST00000216968.4:c.323-256A= ENSP00000216968.3:n.323-256A=
ENST00000635377.1:c.223-256A=
NM_006404.4:c.323-256A= NP_006395.2:n.323-256A=
XM_011528496.1:c.323-256A= XP_011526798.1:n.323-256A=
NM_001355008.1:c.-101-10041T= NP_001341937.1:n.-101-10041T=
NM_006404.5:c.323-256A= MANE Select NP_006395.2:n.323-256A=
NM_001355008.2:c.-101-10041T= NP_001341937.1:n.-101-10041T=
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