Canonical Allele Identifier: CA2677997036
Gene: PRRC2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31622710_31622711insA , CM000668.2:g.31622710_31622711insA GRCh38
NC_000006.11:g.31590487_31590488insA , CM000668.1:g.31590487_31590488insA GRCh37
NC_000006.10:g.31698466_31698467insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376033.3:c.-80_-79insA MANE Select ENSP00000365201.2:n.-80_-79insA
ENST00000376007.8:c.-63-17_-63-16insA ENSP00000365175.4:n.-63-17_-63-16insA
ENST00000376033.2:c.-80_-79insA ENSP00000365201.2:n.-80_-79insA
ENST00000469577.5:n.136-1551_136-1550insA
NM_004638.3:c.-80_-79insA NP_004629.3:n.-80_-79insA
NM_080686.2:c.-63-17_-63-16insA NP_542417.2:n.-63-17_-63-16insA
XM_011514890.1:c.-63-17_-63-16insA XP_011513192.1:n.-63-17_-63-16insA
NM_004638.4:c.-80_-79insA MANE Select NP_004629.3:n.-80_-79insA
NM_080686.3:c.-63-17_-63-16insA NP_542417.2:n.-63-17_-63-16insA