Canonical Allele Identifier: CA136852372

Gene: PRRC2A

Linked Data

• dbSNP Id: rs984381165
• gnomAD v2: 6-31590464-CAGGGGACAGAGACTG-C
• gnomAD v3: 6-31622687-CAGGGGACAGAGACTG-C
• gnomAD v4: 6-31622687-CAGGGGACAGAGACTG-C
• MyVariant Identifiers: chr6:g.31590465_31590479del (hg19) ; chr6:g.31622688_31622702del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622690_31622704del , CM000668.2:g.31622690_31622704del	GRCh38
NC_000006.11:g.31590467_31590481del , CM000668.1:g.31590467_31590481del	GRCh37
NC_000006.10:g.31698446_31698460del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-100_-86del
ENST00000376007.8:c.-63-37_-63-23del	ENSP00000365175.4:n.-63-37_-63-23del
ENST00000376033.2:c.-100_-86del
ENST00000469577.5:n.136-1571_136-1557del
NM_004638.3:c.-100_-86del
NM_080686.2:c.-63-37_-63-23del	NP_542417.2:n.-63-37_-63-23del
XM_011514890.1:c.-63-37_-63-23del	XP_011513192.1:n.-63-37_-63-23del
NM_004638.4:c.-100_-86del
NM_080686.3:c.-63-37_-63-23del	NP_542417.2:n.-63-37_-63-23del