Canonical Allele Identifier: CA2677997005
Gene: PRRC2A HGNC NCBI

Linked Data

gnomAD v4: 6-31622676-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622676T>A , CM000668.2:g.31622676T>A GRCh38
NC_000006.11:g.31590453T>A , CM000668.1:g.31590453T>A GRCh37
NC_000006.10:g.31698432T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-100-14T>A MANE Select ENSP00000365201.2:n.-100-14T>A
ENST00000376007.8:c.-63-51T>A ENSP00000365175.4:n.-63-51T>A
ENST00000376033.2:c.-100-14T>A ENSP00000365201.2:n.-100-14T>A
ENST00000469577.5:n.136-1585T>A
NM_004638.3:c.-100-14T>A NP_004629.3:n.-100-14T>A
NM_080686.2:c.-63-51T>A NP_542417.2:n.-63-51T>A
XM_011514890.1:c.-63-51T>A XP_011513192.1:n.-63-51T>A
NM_004638.4:c.-100-14T>A MANE Select NP_004629.3:n.-100-14T>A
NM_080686.3:c.-63-51T>A NP_542417.2:n.-63-51T>A
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