Canonical Allele Identifier: CA2677997009

Gene: PRRC2A

Linked Data

• gnomAD v4: 6-31622678-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622680del , CM000668.2:g.31622680del	GRCh38
NC_000006.11:g.31590457del , CM000668.1:g.31590457del	GRCh37
NC_000006.10:g.31698436del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-100-10del MANE Select	ENSP00000365201.2:n.-100-10del
ENST00000376007.8:c.-63-47del	ENSP00000365175.4:n.-63-47del
ENST00000376033.2:c.-100-10del	ENSP00000365201.2:n.-100-10del
ENST00000469577.5:n.136-1581del
NM_004638.3:c.-100-10del	NP_004629.3:n.-100-10del
NM_080686.2:c.-63-47del	NP_542417.2:n.-63-47del
XM_011514890.1:c.-63-47del	XP_011513192.1:n.-63-47del
NM_004638.4:c.-100-10del MANE Select	NP_004629.3:n.-100-10del
NM_080686.3:c.-63-47del	NP_542417.2:n.-63-47del