Canonical Allele Identifier: CA635336394
Gene: PROCR HGNC NCBI

Linked Data

dbSNP Id: rs370936992
gnomAD v2: 20-33763702-G-GTTT
gnomAD v3: 20-35175899-G-GTTT
gnomAD v4: 20-35175899-G-GTTT
MyVariant Identifiers: chr20:g.33763703_33763704insTTT (hg19) chr20:g.33763702_33763703insTTT (hg19) chr20:g.35175900_35175901insTTT (hg38) chr20:g.35175899_35175900insTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35175907_35175909dup , CM000682.2:g.35175907_35175909dup GRCh38
NC_000020.10:g.33763710_33763712dup , CM000682.1:g.33763710_33763712dup GRCh37
NC_000020.9:g.33227371_33227373dup NCBI36
NG_032899.1:g.8937_8939dup
NG_032899.2:g.8937_8939dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000216968.5:c.323-261_323-259dup MANE Select ENSP00000216968.3:n.323-261_323-259dup
ENST00000216968.4:c.323-261_323-259dup ENSP00000216968.3:n.323-261_323-259dup
ENST00000635377.1:c.223-261_223-259dup
NM_006404.4:c.323-261_323-259dup NP_006395.2:n.323-261_323-259dup
XM_011528496.1:c.323-261_323-259dup XP_011526798.1:n.323-261_323-259dup
NM_001355008.1:c.-101-10031_-101-10029dup NP_001341937.1:n.-101-10031_-101-10029dup
NM_006404.5:c.323-261_323-259dup MANE Select NP_006395.2:n.323-261_323-259dup
NM_001355008.2:c.-101-10031_-101-10029dup NP_001341937.1:n.-101-10031_-101-10029dup
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