Canonical Allele Identifier: CA2577380366
Gene: PROCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176688T>C , CM000682.2:g.35176688T>C GRCh38
NC_000020.10:g.33764491T>C , CM000682.1:g.33764491T>C GRCh37
NC_000020.9:g.33228152T>C NCBI36
NG_032899.1:g.9718T>C
NG_032899.2:g.9718T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.602-10T>C MANE Select ENSP00000216968.3:n.602-10T>C
ENST00000216968.4:c.602-10T>C ENSP00000216968.3:n.602-10T>C
ENST00000634509.1:c.94+242T>C ENSP00000489456.1:n.94+242T>C
ENST00000635377.1:c.501+242T>C
NM_006404.4:c.602-10T>C NP_006395.2:n.602-10T>C
XM_011528496.1:c.601+242T>C XP_011526798.1:n.601+242T>C
NM_001355008.1:c.-101-10817A>G NP_001341937.1:n.-101-10817A>G
NM_006404.5:c.602-10T>C MANE Select NP_006395.2:n.602-10T>C
NM_001355008.2:c.-101-10817A>G NP_001341937.1:n.-101-10817A>G
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