Canonical Allele Identifier: CA2361537779
Gene: PROCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35175910C= , CM000682.2:g.35175910C= GRCh38
NC_000020.10:g.33763713C= , CM000682.1:g.33763713C= GRCh37
NC_000020.9:g.33227374C= NCBI36
NG_032899.1:g.8940C=
NG_032899.2:g.8940C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.323-258C= MANE Select ENSP00000216968.3:n.323-258C=
ENST00000216968.4:c.323-258C= ENSP00000216968.3:n.323-258C=
ENST00000635377.1:c.223-258C=
NM_006404.4:c.323-258C= NP_006395.2:n.323-258C=
XM_011528496.1:c.323-258C= XP_011526798.1:n.323-258C=
NM_001355008.1:c.-101-10039G= NP_001341937.1:n.-101-10039G=
NM_006404.5:c.323-258C= MANE Select NP_006395.2:n.323-258C=
NM_001355008.2:c.-101-10039G= NP_001341937.1:n.-101-10039G=
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