Canonical Allele Identifier: CA2578566390
Gene: PRRC2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31637437G>C , CM000668.2:g.31637437G>C GRCh38
NC_000006.11:g.31605214G>C , CM000668.1:g.31605214G>C GRCh37
NC_000006.10:g.31713193G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376033.3:c.6334-9G>C MANE Select ENSP00000365201.2:n.6334-9G>C
ENST00000376007.8:c.6334-9G>C ENSP00000365175.4:n.6334-9G>C
ENST00000376033.2:c.6334-9G>C ENSP00000365201.2:n.6334-9G>C
ENST00000462617.1:n.681G>C
ENST00000482441.1:n.394-9G>C
ENST00000492691.5:n.784G>C
NM_004638.3:c.6334-9G>C NP_004629.3:n.6334-9G>C
NM_080686.2:c.6334-9G>C NP_542417.2:n.6334-9G>C
XM_011514890.1:c.6121-9G>C XP_011513192.1:n.6121-9G>C
XM_017011274.1:c.6121-9G>C XP_016866763.1:n.6121-9G>C
NM_004638.4:c.6334-9G>C MANE Select NP_004629.3:n.6334-9G>C
NM_080686.3:c.6334-9G>C NP_542417.2:n.6334-9G>C