Canonical Allele Identifier: CA357836032

Gene: HADH

Linked Data

• MyVariant Identifiers: chr4:g.108948911A>T (hg19) ; chr4:g.108027755A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027755A>T , CM000666.2:g.108027755A>T	GRCh38
NC_000004.11:g.108948911A>T , CM000666.1:g.108948911A>T	GRCh37
NC_000004.10:g.109168360A>T	NCBI36
NG_008156.2:g.42972A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4914A>T
ENST00000510728.6:n.1692A>T
ENST00000514776.3:n.137A>T
ENST00000515462.7:n.1891A>T
ENST00000626637.2:c.716A>T	ENSP00000486771.1:p.Glu239Val
ENST00000638648.2:c.716A>T	ENSP00000507949.1:p.Glu239Val
ENST00000640201.2:n.790A>T
ENST00000640752.2:n.4914A>T
ENST00000682067.1:c.537A>T
ENST00000682086.1:n.773A>T
ENST00000682373.1:c.363A>T
ENST00000684696.1:c.637-184A>T	ENSP00000507675.1:n.637-184A>T
ENST00000309522.8:c.704A>T MANE Select	ENSP00000312288.4:p.Glu235Val
ENST00000403312.6:c.704A>T	ENSP00000385638.3:p.Glu235Val
ENST00000505878.4:c.881A>T	ENSP00000425952.2:p.Glu294Val
ENST00000514776.2:n.137A>T
ENST00000515462.6:n.1891A>T
ENST00000638559.1:c.562A>T
ENST00000638621.1:c.290A>T	ENSP00000491581.1:p.Glu97Val
ENST00000638648.1:n.855A>T
ENST00000639146.1:c.704A>T	ENSP00000492345.1:p.Glu235Val
ENST00000639335.1:c.*139A>T	ENSP00000491310.1:n.*139A>T
ENST00000639698.1:c.516+4192A>T	ENSP00000492420.1:n.516+4192A>T
ENST00000639784.1:c.373+4192A>T
ENST00000640048.1:c.676A>T	ENSP00000492009.1:n.676A>T
ENST00000640060.1:c.*799A>T	ENSP00000492734.1:n.*799A>T
ENST00000640201.1:n.659A>T
ENST00000640752.1:n.4907A>T
ENST00000309522.7:c.704A>T	ENSP00000312288.3:p.Glu235Val
ENST00000403312.5:c.881A>T	ENSP00000385638.2:p.Glu294Val
ENST00000505878.3:c.716A>T	ENSP00000425952.1:p.Glu239Val
ENST00000507260.1:n.404A>T
ENST00000510728.5:n.244A>T
ENST00000515462.5:n.41A>T
ENST00000603302.5:c.704A>T	ENSP00000474560.1:p.Glu235Val
ENST00000626637.1:c.716A>T	ENSP00000486771.1:p.Glu239Val
NM_001184705.2:c.704A>T	NP_001171634.2:p.Glu235Val
NM_005327.4:c.704A>T	NP_005318.3:p.Glu235Val
XM_005262972.1:c.716A>T	XP_005263029.1:p.Glu239Val
XR_938726.1:n.853A>T
NM_001331027.1:c.716A>T	NP_001317956.1:p.Glu239Val
XR_001741214.2:n.798A>T
XR_002959727.1:n.798A>T
NM_001184705.3:c.704A>T	NP_001171634.2:p.Glu235Val
NM_005327.7:c.704A>T MANE Select	NP_005318.6:p.Glu235Val
NM_001184705.4:c.704A>T	NP_001171634.3:p.Glu235Val
NM_001331027.2:c.716A>T	NP_001317956.2:p.Glu239Val