Canonical Allele Identifier: CA440568490

Gene: HADH

Linked Data

• MyVariant Identifiers: chr4:g.108948900C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027744C>T , CM000666.2:g.108027744C>T	GRCh38
NC_000004.11:g.108948900C>T , CM000666.1:g.108948900C>T	GRCh37
NC_000004.10:g.109168349C>T	NCBI36
NG_008156.2:g.42961C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4903C>T
ENST00000510728.6:n.1681C>T
ENST00000514776.3:n.126C>T
ENST00000515462.7:n.1880C>T
ENST00000626637.2:c.705C>T	ENSP00000486771.1:p.Ile235=
ENST00000638648.2:c.705C>T	ENSP00000507949.1:p.Ile235=
ENST00000640201.2:n.779C>T
ENST00000640752.2:n.4903C>T
ENST00000682067.1:c.526C>T
ENST00000682086.1:n.762C>T
ENST00000682373.1:c.352C>T
ENST00000684696.1:c.637-195C>T	ENSP00000507675.1:n.637-195C>T
ENST00000309522.8:c.693C>T MANE Select	ENSP00000312288.4:p.Ile231=
ENST00000403312.6:c.693C>T	ENSP00000385638.3:p.Ile231=
ENST00000505878.4:c.870C>T	ENSP00000425952.2:p.Ile290=
ENST00000514776.2:n.126C>T
ENST00000515462.6:n.1880C>T
ENST00000638559.1:c.551C>T
ENST00000638621.1:c.279C>T	ENSP00000491581.1:p.Ile93=
ENST00000638648.1:n.844C>T
ENST00000639146.1:c.693C>T	ENSP00000492345.1:p.Ile231=
ENST00000639335.1:c.*128C>T	ENSP00000491310.1:n.*128C>T
ENST00000639698.1:c.516+4181C>T	ENSP00000492420.1:n.516+4181C>T
ENST00000639784.1:c.373+4181C>T
ENST00000640048.1:c.665C>T	ENSP00000492009.1:n.665C>T
ENST00000640060.1:c.*788C>T	ENSP00000492734.1:n.*788C>T
ENST00000640201.1:n.648C>T
ENST00000640752.1:n.4896C>T
ENST00000309522.7:c.693C>T	ENSP00000312288.3:p.Ile231=
ENST00000403312.5:c.870C>T	ENSP00000385638.2:p.Ile290=
ENST00000505878.3:c.705C>T	ENSP00000425952.1:p.Ile235=
ENST00000507260.1:n.393C>T
ENST00000510728.5:n.233C>T
ENST00000515462.5:n.30C>T
ENST00000603302.5:c.693C>T	ENSP00000474560.1:p.Ile231=
ENST00000626637.1:c.705C>T	ENSP00000486771.1:p.Ile235=
NM_001184705.2:c.693C>T	NP_001171634.2:p.Ile231=
NM_005327.4:c.693C>T	NP_005318.3:p.Ile231=
XM_005262972.1:c.705C>T	XP_005263029.1:p.Ile235=
XR_938726.1:n.842C>T
NM_001331027.1:c.705C>T	NP_001317956.1:p.Ile235=
XR_001741214.2:n.787C>T
XR_002959727.1:n.787C>T
NM_001184705.3:c.693C>T	NP_001171634.2:p.Ile231=
NM_005327.7:c.693C>T MANE Select	NP_005318.6:p.Ile231=
NM_001184705.4:c.693C>T	NP_001171634.3:p.Ile231=
NM_001331027.2:c.705C>T	NP_001317956.2:p.Ile235=