Canonical Allele Identifier: CA1017161439
Gene: PROCR HGNC NCBI

Linked Data

dbSNP Id: rs1600734392
gnomAD v3: 20-35175734-G-A
gnomAD v4: 20-35175734-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35175734G>A , CM000682.2:g.35175734G>A GRCh38
NC_000020.10:g.33763537G>A , CM000682.1:g.33763537G>A GRCh37
NC_000020.9:g.33227198G>A NCBI36
NG_032899.1:g.8764G>A
NG_032899.2:g.8764G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.323-434G>A MANE Select ENSP00000216968.3:n.323-434G>A
ENST00000216968.4:c.323-434G>A ENSP00000216968.3:n.323-434G>A
ENST00000635377.1:c.223-434G>A
NM_006404.4:c.323-434G>A NP_006395.2:n.323-434G>A
XM_011528496.1:c.323-434G>A XP_011526798.1:n.323-434G>A
NM_001355008.1:c.-101-9863C>T NP_001341937.1:n.-101-9863C>T
NM_006404.5:c.323-434G>A MANE Select NP_006395.2:n.323-434G>A
NM_001355008.2:c.-101-9863C>T NP_001341937.1:n.-101-9863C>T
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