Canonical Allele Identifier: CA566355391

Gene: PRRC2A

Linked Data

• dbSNP Id: rs1461354641
• gnomAD v2: 6-31590527-TGCC-T
• MyVariant Identifiers: chr6:g.31590528_31590530del (hg19) ; chr6:g.31622751_31622753del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622751_31622753del , CM000668.2:g.31622751_31622753del	GRCh38
NC_000006.11:g.31590528_31590530del , CM000668.1:g.31590528_31590530del	GRCh37
NC_000006.10:g.31698507_31698509del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.-39_-37del MANE Select	ENSP00000365201.2:n.-39_-37del
ENST00000376007.8:c.-39_-37del	ENSP00000365175.4:n.-39_-37del
ENST00000376033.2:c.-39_-37del	ENSP00000365201.2:n.-39_-37del
ENST00000469577.5:n.136-1510_136-1508del
NM_004638.3:c.-39_-37del	NP_004629.3:n.-39_-37del
NM_080686.2:c.-39_-37del	NP_542417.2:n.-39_-37del
XM_011514890.1:c.-39_-37del	XP_011513192.1:n.-39_-37del
NM_004638.4:c.-39_-37del MANE Select	NP_004629.3:n.-39_-37del
NM_080686.3:c.-39_-37del	NP_542417.2:n.-39_-37del