Canonical Allele Identifier: CA1483969387

Gene: HADH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027728A= , CM000666.2:g.108027728A=	GRCh38
NC_000004.11:g.108948884A= , CM000666.1:g.108948884A=	GRCh37
NC_000004.10:g.109168333A=	NCBI36
NG_008156.2:g.42945A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4887A=
ENST00000510728.6:n.1665A=
ENST00000514776.3:n.110A=
ENST00000515462.7:n.1864A=
ENST00000626637.2:c.689A=	ENSP00000486771.1:p.Tyr230=
ENST00000638648.2:c.689A=	ENSP00000507949.1:p.Tyr230=
ENST00000640201.2:n.763A=
ENST00000640752.2:n.4887A=
ENST00000682067.1:c.510A=
ENST00000682086.1:n.746A=
ENST00000682373.1:c.336A=
ENST00000684696.1:c.637-211A=	ENSP00000507675.1:n.637-211A=
ENST00000309522.8:c.677A= MANE Select	ENSP00000312288.4:p.Tyr226=
ENST00000403312.6:c.677A=	ENSP00000385638.3:p.Tyr226=
ENST00000505878.4:c.854A=	ENSP00000425952.2:p.Tyr285=
ENST00000514776.2:n.110A=
ENST00000515462.6:n.1864A=
ENST00000638559.1:c.535A=
ENST00000638621.1:c.263A=	ENSP00000491581.1:p.Tyr88=
ENST00000638648.1:n.828A=
ENST00000639146.1:c.677A=	ENSP00000492345.1:p.Tyr226=
ENST00000639335.1:c.*112A=	ENSP00000491310.1:n.*112A=
ENST00000639698.1:c.516+4165A=	ENSP00000492420.1:n.516+4165A=
ENST00000639784.1:c.373+4165A=
ENST00000640048.1:c.649A=	ENSP00000492009.1:n.649A=
ENST00000640060.1:c.*772A=	ENSP00000492734.1:n.*772A=
ENST00000640201.1:n.632A=
ENST00000640752.1:n.4880A=
ENST00000309522.7:c.677A=	ENSP00000312288.3:p.Tyr226=
ENST00000403312.5:c.854A=	ENSP00000385638.2:p.Tyr285=
ENST00000505878.3:c.689A=	ENSP00000425952.1:p.Tyr230=
ENST00000507260.1:n.377A=
ENST00000510728.5:n.217A=
ENST00000515462.5:n.14A=
ENST00000603302.5:c.677A=	ENSP00000474560.1:p.Tyr226=
ENST00000626637.1:c.689A=	ENSP00000486771.1:p.Tyr230=
NM_001184705.2:c.677A=	NP_001171634.2:p.Tyr226=
NM_005327.4:c.677A=	NP_005318.3:p.Tyr226=
XM_005262972.1:c.689A=	XP_005263029.1:p.Tyr230=
XR_938726.1:n.826A=
NM_001331027.1:c.689A=	NP_001317956.1:p.Tyr230=
XR_001741214.2:n.771A=
XR_002959727.1:n.771A=
NM_001184705.3:c.677A=	NP_001171634.2:p.Tyr226=
NM_005327.7:c.677A= MANE Select	NP_005318.6:p.Tyr226=
NM_001184705.4:c.677A=	NP_001171634.3:p.Tyr226=
NM_001331027.2:c.689A=	NP_001317956.2:p.Tyr230=