Canonical Allele Identifier: CA476791629

Gene: DLAT PIH1D2

Linked Data

• dbSNP Id: rs1592734570
• gnomAD v4: 11-112061004-AAC-A
• MyVariant Identifiers: chr11:g.111931729_111931730del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112061005_112061006del , CM000673.2:g.112061005_112061006del	GRCh38
NC_000011.9:g.111931729_111931730del , CM000673.1:g.111931729_111931730del	GRCh37
NC_000011.8:g.111436939_111436940del	NCBI36
NG_013342.1:g.41192_41193del

Transcript Alleles

HGVS	Amino-acid change
ENST00000713569.1:c.1678-33_1678-32del (DLAT)	ENSP00000518862.1:n.1678-33_1678-32del
ENST00000280346.11:c.1678-33_1678-32del (DLAT) MANE Select	ENSP00000280346.7:n.1678-33_1678-32del
ENST00000527231.2:n.1725-33_1725-32del (DLAT)
ENST00000531306.2:c.1297-33_1297-32del (DLAT)	ENSP00000433432.2:n.1297-33_1297-32del
ENST00000679368.1:c.*605-33_*605-32del (DLAT)	ENSP00000505314.1:n.*605-33_*605-32del
ENST00000679614.1:c.1075-33_1075-32del (DLAT)	ENSP00000506007.1:n.1075-33_1075-32del
ENST00000679815.1:c.*1111-33_*1111-32del (DLAT)	ENSP00000504880.1:n.*1111-33_*1111-32del
ENST00000679878.1:c.1645-33_1645-32del (DLAT)	ENSP00000505567.1:n.1645-33_1645-32del
ENST00000680010.1:c.*819-33_*819-32del (DLAT)	ENSP00000505768.1:n.*819-33_*819-32del
ENST00000680154.1:n.1009-33_1009-32del (DLAT)
ENST00000680331.1:c.1399-33_1399-32del (DLAT)	ENSP00000506707.1:n.1399-33_1399-32del
ENST00000680411.1:c.1423-33_1423-32del (DLAT)	ENSP00000505915.1:n.1423-33_1423-32del
ENST00000681316.1:c.1672-33_1672-32del (DLAT)	ENSP00000506560.1:n.1672-33_1672-32del
ENST00000681328.1:c.1657-33_1657-32del (DLAT)	ENSP00000506355.1:n.1657-33_1657-32del
ENST00000681339.1:c.1570-33_1570-32del (DLAT)	ENSP00000506167.1:n.1570-33_1570-32del
ENST00000681638.1:c.*1031-33_*1031-32del (DLAT)	ENSP00000506090.1:n.*1031-33_*1031-32del
ENST00000280346.10:c.1678-33_1678-32del (DLAT)	ENSP00000280346.6:n.1678-33_1678-32del
ENST00000393051.5:c.1363-33_1363-32del (DLAT)	ENSP00000376771.1:n.1363-33_1363-32del
ENST00000527231.1:n.72-33_72-32del (DLAT)
ENST00000531306.1:c.1174-33_1174-32del (DLAT)	ENSP00000433432.1:n.1174-33_1174-32del
ENST00000533297.1:c.*1353-33_*1353-32del (DLAT)	ENSP00000435374.1:n.*1353-33_*1353-32del
NM_001931.4:c.1678-33_1678-32del (DLAT)	NP_001922.2:n.1678-33_1678-32del
XM_011542590.1:c.814-212_814-211del (PIH1D2)	XP_011540892.1:n.814-212_814-211del
XM_011542592.1:c.814-8319_814-8318del (PIH1D2)	XP_011540894.1:n.814-8319_814-8318del
XM_011542647.1:c.1570-33_1570-32del (DLAT)	XP_011540949.1:n.1570-33_1570-32del
XM_011542647.3:c.1570-33_1570-32del (DLAT)	XP_011540949.1:n.1570-33_1570-32del
XM_017017202.2:c.814-5226_814-5225del (PIH1D2)	XP_016872691.1:n.814-5226_814-5225del
XM_017017203.2:c.814-212_814-211del (PIH1D2)	XP_016872692.1:n.814-212_814-211del
XM_017017204.2:c.814-5255_814-5254del (PIH1D2)	XP_016872693.1:n.814-5255_814-5254del
XM_017017205.2:c.814-8319_814-8318del (PIH1D2)	XP_016872694.1:n.814-8319_814-8318del
NM_001372031.1:c.1696-33_1696-32del (DLAT)	NP_001358960.1:n.1696-33_1696-32del
NM_001372032.1:c.1672-33_1672-32del (DLAT)	NP_001358961.1:n.1672-33_1672-32del
NM_001372033.1:c.1657-33_1657-32del (DLAT)	NP_001358962.1:n.1657-33_1657-32del
NM_001372034.1:c.1645-33_1645-32del (DLAT)	NP_001358963.1:n.1645-33_1645-32del
NM_001372035.1:c.1570-33_1570-32del (DLAT)	NP_001358964.1:n.1570-33_1570-32del
NM_001372036.1:c.1552-33_1552-32del (DLAT)	NP_001358965.1:n.1552-33_1552-32del
NM_001372037.1:c.1510-33_1510-32del (DLAT)	NP_001358966.1:n.1510-33_1510-32del
NM_001372038.1:c.1399-33_1399-32del (DLAT)	NP_001358967.1:n.1399-33_1399-32del
NM_001372039.1:c.1363-33_1363-32del (DLAT)	NP_001358968.1:n.1363-33_1363-32del
NM_001372040.1:c.1297-33_1297-32del (DLAT)	NP_001358969.1:n.1297-33_1297-32del
NM_001372041.1:c.1255-33_1255-32del (DLAT)	NP_001358970.1:n.1255-33_1255-32del
NM_001372042.1:c.1216-33_1216-32del (DLAT)	NP_001358971.1:n.1216-33_1216-32del
NM_001931.5:c.1678-33_1678-32del (DLAT) MANE Select	NP_001922.2:n.1678-33_1678-32del
NR_164072.1:n.1555-33_1555-32del (DLAT)