Canonical Allele Identifier: CA2816230997
Gene: PROCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35176681C>A , CM000682.2:g.35176681C>A GRCh38
NC_000020.10:g.33764484C>A , CM000682.1:g.33764484C>A GRCh37
NC_000020.9:g.33228145C>A NCBI36
NG_032899.1:g.9711C>A
NG_032899.2:g.9711C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.602-17C>A MANE Select ENSP00000216968.3:n.602-17C>A
ENST00000216968.4:c.602-17C>A ENSP00000216968.3:n.602-17C>A
ENST00000634509.1:c.94+235C>A ENSP00000489456.1:n.94+235C>A
ENST00000635377.1:c.501+235C>A
NM_006404.4:c.602-17C>A NP_006395.2:n.602-17C>A
XM_011528496.1:c.601+235C>A XP_011526798.1:n.601+235C>A
NM_001355008.1:c.-101-10810G>T NP_001341937.1:n.-101-10810G>T
NM_006404.5:c.602-17C>A MANE Select NP_006395.2:n.602-17C>A
NM_001355008.2:c.-101-10810G>T NP_001341937.1:n.-101-10810G>T
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