Canonical Allele Identifier: CA2677999726

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31637437-G-A

Genomic Alleles

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

Transcript Alleles

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