Canonical Allele Identifier: CA363364738

Gene: PRRC2A

Linked Data

• dbSNP Id: rs771738803
• gnomAD v4: 6-31635196-A-C
• MyVariant Identifiers: chr6:g.31602973A>C (hg19) ; chr6:g.31635196A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31635196A>C , CM000668.2:g.31635196A>C	GRCh38
NC_000006.11:g.31602973A>C , CM000668.1:g.31602973A>C	GRCh37
NC_000006.10:g.31710952A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376033.3:c.5225A>C MANE Select	ENSP00000365201.2:p.Asp1742Ala
ENST00000376007.8:c.5225A>C	ENSP00000365175.4:p.Asp1742Ala
ENST00000376033.2:c.5225A>C	ENSP00000365201.2:p.Asp1742Ala
ENST00000484787.1:n.636A>C
NM_004638.3:c.5225A>C	NP_004629.3:p.Asp1742Ala
NM_080686.2:c.5225A>C	NP_542417.2:p.Asp1742Ala
XM_011514890.1:c.5225A>C	XP_011513192.1:p.Asp1742Ala
XM_017011274.1:c.5225A>C	XP_016866763.1:p.Asp1742Ala
NM_004638.4:c.5225A>C MANE Select	NP_004629.3:p.Asp1742Ala
NM_080686.3:c.5225A>C	NP_542417.2:p.Asp1742Ala