Canonical Allele Identifier: CA2677999724

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31637430-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31637431_31637432del , CM000668.2:g.31637431_31637432del	GRCh38
NC_000006.11:g.31605208_31605209del , CM000668.1:g.31605208_31605209del	GRCh37
NC_000006.10:g.31713187_31713188del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.6334-15_6334-14del MANE Select	ENSP00000365201.2:n.6334-15_6334-14del
ENST00000376007.8:c.6334-15_6334-14del	ENSP00000365175.4:n.6334-15_6334-14del
ENST00000376033.2:c.6334-15_6334-14del	ENSP00000365201.2:n.6334-15_6334-14del
ENST00000462617.1:n.675_676del
ENST00000482441.1:n.394-15_394-14del
ENST00000492691.5:n.778_779del
NM_004638.3:c.6334-15_6334-14del	NP_004629.3:n.6334-15_6334-14del
NM_080686.2:c.6334-15_6334-14del	NP_542417.2:n.6334-15_6334-14del
XM_011514890.1:c.6121-15_6121-14del	XP_011513192.1:n.6121-15_6121-14del
XM_017011274.1:c.6121-15_6121-14del	XP_016866763.1:n.6121-15_6121-14del
NM_004638.4:c.6334-15_6334-14del MANE Select	NP_004629.3:n.6334-15_6334-14del
NM_080686.3:c.6334-15_6334-14del	NP_542417.2:n.6334-15_6334-14del