Canonical Allele Identifier: CA2578565759

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31622775-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622775T>G , CM000668.2:g.31622775T>G	GRCh38
NC_000006.11:g.31590552T>G , CM000668.1:g.31590552T>G	GRCh37
NC_000006.10:g.31698531T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706625.1:c.2T>G	ENSP00000516471.1:p.Met1Arg
ENST00000376033.3:c.-15T>G MANE Select	ENSP00000365201.2:n.-15T>G
ENST00000376007.8:c.-15T>G	ENSP00000365175.4:n.-15T>G
ENST00000376033.2:c.-15T>G	ENSP00000365201.2:n.-15T>G
ENST00000469577.5:n.136-1486T>G
NM_004638.3:c.-15T>G	NP_004629.3:n.-15T>G
NM_080686.2:c.-15T>G	NP_542417.2:n.-15T>G
XM_011514890.1:c.-15T>G	XP_011513192.1:n.-15T>G
NM_004638.4:c.-15T>G MANE Select	NP_004629.3:n.-15T>G
NM_080686.3:c.-15T>G	NP_542417.2:n.-15T>G