Canonical Allele Identifier: CA449661980

Gene: PRRC2A

Linked Data

• MyVariant Identifiers: chr6:g.31590635T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622858T>C , CM000668.2:g.31622858T>C	GRCh38
NC_000006.11:g.31590635T>C , CM000668.1:g.31590635T>C	GRCh37
NC_000006.10:g.31698614T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706625.1:c.85T>C	ENSP00000516471.1:p.Ter29Arg
ENST00000376033.3:c.69T>C MANE Select	ENSP00000365201.2:p.Phe23=
ENST00000376007.8:c.69T>C	ENSP00000365175.4:p.Phe23=
ENST00000376033.2:c.69T>C	ENSP00000365201.2:p.Phe23=
ENST00000469577.5:n.136-1403T>C
NM_004638.3:c.69T>C	NP_004629.3:p.Phe23=
NM_080686.2:c.69T>C	NP_542417.2:p.Phe23=
XM_011514890.1:c.69T>C	XP_011513192.1:p.Phe23=
XM_017011274.1:c.69T>C	XP_016866763.1:p.Phe23=
NM_004638.4:c.69T>C MANE Select	NP_004629.3:p.Phe23=
NM_080686.3:c.69T>C	NP_542417.2:p.Phe23=