Canonical Allele Identifier: CA449661979

Gene: PRRC2A

Linked Data

• MyVariant Identifiers: chr6:g.31590632G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31622855G>T , CM000668.2:g.31622855G>T	GRCh38
NC_000006.11:g.31590632G>T , CM000668.1:g.31590632G>T	GRCh37
NC_000006.10:g.31698611G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706625.1:c.82G>T	ENSP00000516471.1:p.Val28Phe
ENST00000376033.3:c.66G>T MANE Select	ENSP00000365201.2:p.Leu22=
ENST00000376007.8:c.66G>T	ENSP00000365175.4:p.Leu22=
ENST00000376033.2:c.66G>T	ENSP00000365201.2:p.Leu22=
ENST00000469577.5:n.136-1406G>T
NM_004638.3:c.66G>T	NP_004629.3:p.Leu22=
NM_080686.2:c.66G>T	NP_542417.2:p.Leu22=
XM_011514890.1:c.66G>T	XP_011513192.1:p.Leu22=
XM_017011274.1:c.66G>T	XP_016866763.1:p.Leu22=
NM_004638.4:c.66G>T MANE Select	NP_004629.3:p.Leu22=
NM_080686.3:c.66G>T	NP_542417.2:p.Leu22=