Canonical Allele Identifier: CA2677997007
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31622677-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622677A>G , CM000668.2:g.31622677A>G GRCh38
NC_000006.11:g.31590454A>G , CM000668.1:g.31590454A>G GRCh37
NC_000006.10:g.31698433A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-100-13A>G MANE Select ENSP00000365201.2:n.-100-13A>G
ENST00000376007.8:c.-63-50A>G ENSP00000365175.4:n.-63-50A>G
ENST00000376033.2:c.-100-13A>G ENSP00000365201.2:n.-100-13A>G
ENST00000469577.5:n.136-1584A>G
NM_004638.3:c.-100-13A>G NP_004629.3:n.-100-13A>G
NM_080686.2:c.-63-50A>G NP_542417.2:n.-63-50A>G
XM_011514890.1:c.-63-50A>G XP_011513192.1:n.-63-50A>G
NM_004638.4:c.-100-13A>G MANE Select NP_004629.3:n.-100-13A>G
NM_080686.3:c.-63-50A>G NP_542417.2:n.-63-50A>G
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