Canonical Allele Identifier: CA399857739

Gene: ACBD4

Linked Data

• MyVariant Identifiers: chr17:g.43220905G>A (hg19) ; chr17:g.45143538G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45143538G>A , CM000679.2:g.45143538G>A	GRCh38
NC_000017.10:g.43220905G>A , CM000679.1:g.43220905G>A	GRCh37
NC_000017.9:g.40576688G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321854.13:c.885G>A MANE Select	ENSP00000314440.8:p.Trp295Ter
ENST00000321854.12:c.885G>A	ENSP00000314440.8:p.Trp295Ter
ENST00000398322.7:c.885G>A	ENSP00000381367.2:p.Trp295Ter
ENST00000431281.5:c.923G>A	ENSP00000405969.1:p.Gly308Asp
ENST00000585553.5:n.1603G>A
ENST00000586346.5:c.923G>A	ENSP00000465484.1:p.Gly308Asp
ENST00000591859.5:c.923G>A	ENSP00000465610.1:p.Gly308Asp
ENST00000592162.5:c.745G>A	ENSP00000466305.1:p.Ala249Thr
NM_001135704.1:c.923G>A	NP_001129176.1:p.Gly308Asp
NM_001135705.1:c.885G>A	NP_001129177.1:p.Trp295Ter
NM_001135706.1:c.923G>A	NP_001129178.1:p.Gly308Asp
NM_024722.2:c.885G>A	NP_078998.1:p.Trp295Ter
XM_005257673.1:c.926G>A	XP_005257730.1:p.Gly309Asp
XM_005257674.1:c.926G>A	XP_005257731.1:p.Gly309Asp
XM_005257677.1:c.923G>A	XP_005257734.1:p.Gly308Asp
XM_006722085.1:c.888G>A	XP_006722148.1:p.Trp296Ter
XM_006722088.1:c.786G>A	XP_006722151.1:p.Trp262Ter
XM_006722089.1:c.748G>A	XP_006722152.1:p.Ala250Thr
XM_006722090.1:c.745G>A	XP_006722153.1:p.Ala249Thr
XM_011525255.1:c.926G>A	XP_011523557.1:p.Gly309Asp
XM_011525256.1:c.926G>A	XP_011523558.1:p.Gly309Asp
XM_011525257.1:c.783G>A	XP_011523559.1:p.Trp261Ter
NM_001135705.2:c.885G>A	NP_001129177.1:p.Trp295Ter
NM_001135706.2:c.923G>A	NP_001129178.1:p.Gly308Asp
NM_001135707.2:c.*928G>A	NP_001129179.1:n.*928G>A
NM_001321352.1:c.923G>A	NP_001308281.1:p.Gly308Asp
NM_001321353.1:c.923G>A	NP_001308282.1:p.Gly308Asp
NM_024722.3:c.885G>A	NP_078998.1:p.Trp295Ter
XM_006722085.2:c.888G>A	XP_006722148.1:p.Trp296Ter
XM_017025084.1:c.944G>A	XP_016880573.1:p.Gly315Asp
XM_017025085.1:c.944G>A	XP_016880574.1:p.Gly315Asp
XM_017025086.1:c.944G>A	XP_016880575.1:p.Gly315Asp
XM_017025087.1:c.926G>A	XP_016880576.1:p.Gly309Asp
XM_017025088.1:c.923G>A	XP_016880577.1:p.Gly308Asp
XM_017025089.2:c.*758G>A	XP_016880578.1:n.*758G>A
XM_017025090.1:c.906G>A	XP_016880579.1:p.Trp302Ter
XM_017025091.1:c.885G>A	XP_016880580.1:p.Trp295Ter
XM_017025092.2:c.885G>A	XP_016880581.1:p.Trp295Ter
XM_017025094.1:c.*928G>A	XP_016880583.1:n.*928G>A
XM_017025095.1:c.804G>A	XP_016880584.1:p.Trp268Ter
XM_017025096.1:c.766G>A	XP_016880585.1:p.Ala256Thr
XM_017025097.1:c.783G>A	XP_016880586.1:p.Trp261Ter
XM_017025098.1:c.783G>A	XP_016880587.1:p.Trp261Ter
XM_017025099.1:c.745G>A	XP_016880588.1:p.Ala249Thr
XM_024450949.1:c.*758G>A	XP_024306717.1:n.*758G>A
NM_001135705.3:c.885G>A MANE Select	NP_001129177.1:p.Trp295Ter
NM_001135706.3:c.923G>A	NP_001129178.1:p.Gly308Asp
NM_001135707.3:c.*928G>A	NP_001129179.1:n.*928G>A
NM_001321352.2:c.923G>A	NP_001308281.1:p.Gly308Asp
NM_001321353.2:c.923G>A	NP_001308282.1:p.Gly308Asp
NM_024722.4:c.885G>A	NP_078998.1:p.Trp295Ter
NM_001378111.1:c.*928G>A	NP_001365040.1:n.*928G>A
NM_001378112.1:c.*928G>A	NP_001365041.1:n.*928G>A