Canonical Allele Identifier: CA2677997030

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31622701-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622704_31622705del , CM000668.2:g.31622704_31622705del	GRCh38
NC_000006.11:g.31590481_31590482del , CM000668.1:g.31590481_31590482del	GRCh37
NC_000006.10:g.31698460_31698461del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-86_-85del MANE Select	ENSP00000365201.2:n.-86_-85del
ENST00000376007.8:c.-63-23_-63-22del	ENSP00000365175.4:n.-63-23_-63-22del
ENST00000376033.2:c.-86_-85del	ENSP00000365201.2:n.-86_-85del
ENST00000469577.5:n.136-1557_136-1556del
NM_004638.3:c.-86_-85del	NP_004629.3:n.-86_-85del
NM_080686.2:c.-63-23_-63-22del	NP_542417.2:n.-63-23_-63-22del
XM_011514890.1:c.-63-23_-63-22del	XP_011513192.1:n.-63-23_-63-22del
NM_004638.4:c.-86_-85del MANE Select	NP_004629.3:n.-86_-85del
NM_080686.3:c.-63-23_-63-22del	NP_542417.2:n.-63-23_-63-22del