Canonical Allele Identifier: CA382618179

Gene: DLAT PIH1D2

Linked Data

• MyVariant Identifiers: chr11:g.111931798G>T (hg19) ; chr11:g.112061074G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112061074G>T , CM000673.2:g.112061074G>T	GRCh38
NC_000011.9:g.111931798G>T , CM000673.1:g.111931798G>T	GRCh37
NC_000011.8:g.111437008G>T	NCBI36
NG_013342.1:g.41261G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713569.1:c.1714G>T (DLAT)	ENSP00000518862.1:p.Gly572Ter
ENST00000280346.11:c.1714G>T (DLAT) MANE Select	ENSP00000280346.7:p.Gly572Ter
ENST00000527231.2:n.1761G>T (DLAT)
ENST00000531306.2:c.1333G>T (DLAT)	ENSP00000433432.2:p.Gly445Ter
ENST00000679368.1:c.*641G>T (DLAT)	ENSP00000505314.1:n.*641G>T
ENST00000679614.1:c.1111G>T (DLAT)	ENSP00000506007.1:p.Gly371Ter
ENST00000679815.1:c.*1147G>T (DLAT)	ENSP00000504880.1:n.*1147G>T
ENST00000679878.1:c.1681G>T (DLAT)	ENSP00000505567.1:p.Gly561Ter
ENST00000680010.1:c.*855G>T (DLAT)	ENSP00000505768.1:n.*855G>T
ENST00000680154.1:n.1045G>T (DLAT)
ENST00000680331.1:c.1435G>T (DLAT)	ENSP00000506707.1:p.Gly479Ter
ENST00000680411.1:c.1459G>T (DLAT)	ENSP00000505915.1:p.Gly487Ter
ENST00000681316.1:c.1708G>T (DLAT)	ENSP00000506560.1:p.Gly570Ter
ENST00000681328.1:c.1693G>T (DLAT)	ENSP00000506355.1:p.Gly565Ter
ENST00000681339.1:c.1606G>T (DLAT)	ENSP00000506167.1:p.Gly536Ter
ENST00000681638.1:c.*1067G>T (DLAT)	ENSP00000506090.1:n.*1067G>T
ENST00000280346.10:c.1714G>T (DLAT)	ENSP00000280346.6:p.Gly572Ter
ENST00000393051.5:c.1399G>T (DLAT)	ENSP00000376771.1:p.Gly467Ter
ENST00000527231.1:n.108G>T (DLAT)
ENST00000531306.1:c.1210G>T (DLAT)	ENSP00000433432.1:p.Gly404Ter
ENST00000533297.1:c.*1389G>T (DLAT)	ENSP00000435374.1:n.*1389G>T
NM_001931.4:c.1714G>T (DLAT)	NP_001922.2:p.Gly572Ter
XM_011542590.1:c.814-280C>A (PIH1D2)	XP_011540892.1:n.814-280C>A
XM_011542592.1:c.814-8387C>A (PIH1D2)	XP_011540894.1:n.814-8387C>A
XM_011542647.1:c.1606G>T (DLAT)	XP_011540949.1:p.Gly536Ter
XM_011542647.3:c.1606G>T (DLAT)	XP_011540949.1:p.Gly536Ter
XM_017017202.2:c.814-5294C>A (PIH1D2)	XP_016872691.1:n.814-5294C>A
XM_017017203.2:c.814-280C>A (PIH1D2)	XP_016872692.1:n.814-280C>A
XM_017017204.2:c.814-5323C>A (PIH1D2)	XP_016872693.1:n.814-5323C>A
XM_017017205.2:c.814-8387C>A (PIH1D2)	XP_016872694.1:n.814-8387C>A
NM_001372031.1:c.1732G>T (DLAT)	NP_001358960.1:p.Gly578Ter
NM_001372032.1:c.1708G>T (DLAT)	NP_001358961.1:p.Gly570Ter
NM_001372033.1:c.1693G>T (DLAT)	NP_001358962.1:p.Gly565Ter
NM_001372034.1:c.1681G>T (DLAT)	NP_001358963.1:p.Gly561Ter
NM_001372035.1:c.1606G>T (DLAT)	NP_001358964.1:p.Gly536Ter
NM_001372036.1:c.1588G>T (DLAT)	NP_001358965.1:p.Gly530Ter
NM_001372037.1:c.1546G>T (DLAT)	NP_001358966.1:p.Gly516Ter
NM_001372038.1:c.1435G>T (DLAT)	NP_001358967.1:p.Gly479Ter
NM_001372039.1:c.1399G>T (DLAT)	NP_001358968.1:p.Gly467Ter
NM_001372040.1:c.1333G>T (DLAT)	NP_001358969.1:p.Gly445Ter
NM_001372041.1:c.1291G>T (DLAT)	NP_001358970.1:p.Gly431Ter
NM_001372042.1:c.1252G>T (DLAT)	NP_001358971.1:p.Gly418Ter
NM_001931.5:c.1714G>T (DLAT) MANE Select	NP_001922.2:p.Gly572Ter
NR_164072.1:n.1591G>T (DLAT)