Canonical Allele Identifier: CA357835893

Gene: HADH

Linked Data

• MyVariant Identifiers: chr4:g.108948874C>G (hg19) ; chr4:g.108027718C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027718C>G , CM000666.2:g.108027718C>G	GRCh38
NC_000004.11:g.108948874C>G , CM000666.1:g.108948874C>G	GRCh37
NC_000004.10:g.109168323C>G	NCBI36
NG_008156.2:g.42935C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4877C>G
ENST00000510728.6:n.1655C>G
ENST00000514776.3:n.100C>G
ENST00000515462.7:n.1854C>G
ENST00000626637.2:c.679C>G	ENSP00000486771.1:p.Leu227Val
ENST00000638648.2:c.679C>G	ENSP00000507949.1:p.Leu227Val
ENST00000640201.2:n.753C>G
ENST00000640752.2:n.4877C>G
ENST00000682067.1:c.500C>G
ENST00000682086.1:n.736C>G
ENST00000682373.1:c.326C>G
ENST00000684696.1:c.637-221C>G	ENSP00000507675.1:n.637-221C>G
ENST00000309522.8:c.667C>G MANE Select	ENSP00000312288.4:p.Leu223Val
ENST00000403312.6:c.667C>G	ENSP00000385638.3:p.Leu223Val
ENST00000505878.4:c.844C>G	ENSP00000425952.2:p.Leu282Val
ENST00000514776.2:n.100C>G
ENST00000515462.6:n.1854C>G
ENST00000638559.1:c.525C>G
ENST00000638621.1:c.253C>G	ENSP00000491581.1:p.Leu85Val
ENST00000638648.1:n.818C>G
ENST00000639146.1:c.667C>G	ENSP00000492345.1:p.Leu223Val
ENST00000639335.1:c.*102C>G	ENSP00000491310.1:n.*102C>G
ENST00000639698.1:c.516+4155C>G	ENSP00000492420.1:n.516+4155C>G
ENST00000639784.1:c.373+4155C>G
ENST00000640048.1:c.639C>G	ENSP00000492009.1:n.639C>G
ENST00000640060.1:c.*762C>G	ENSP00000492734.1:n.*762C>G
ENST00000640201.1:n.622C>G
ENST00000640752.1:n.4870C>G
ENST00000309522.7:c.667C>G	ENSP00000312288.3:p.Leu223Val
ENST00000403312.5:c.844C>G	ENSP00000385638.2:p.Leu282Val
ENST00000505878.3:c.679C>G	ENSP00000425952.1:p.Leu227Val
ENST00000507260.1:n.367C>G
ENST00000510728.5:n.207C>G
ENST00000515462.5:n.4C>G
ENST00000603302.5:c.667C>G	ENSP00000474560.1:p.Leu223Val
ENST00000626637.1:c.679C>G	ENSP00000486771.1:p.Leu227Val
NM_001184705.2:c.667C>G	NP_001171634.2:p.Leu223Val
NM_005327.4:c.667C>G	NP_005318.3:p.Leu223Val
XM_005262972.1:c.679C>G	XP_005263029.1:p.Leu227Val
XR_938726.1:n.816C>G
NM_001331027.1:c.679C>G	NP_001317956.1:p.Leu227Val
XR_001741214.2:n.761C>G
XR_002959727.1:n.761C>G
NM_001184705.3:c.667C>G	NP_001171634.2:p.Leu223Val
NM_005327.7:c.667C>G MANE Select	NP_005318.6:p.Leu223Val
NM_001184705.4:c.667C>G	NP_001171634.3:p.Leu223Val
NM_001331027.2:c.679C>G	NP_001317956.2:p.Leu227Val