Canonical Allele Identifier: CA357835996

Gene: HADH

Linked Data

• gnomAD v4: 4-108027745-A-G
• MyVariant Identifiers: chr4:g.108948901A>G (hg19) ; chr4:g.108027745A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027745A>G , CM000666.2:g.108027745A>G	GRCh38
NC_000004.11:g.108948901A>G , CM000666.1:g.108948901A>G	GRCh37
NC_000004.10:g.109168350A>G	NCBI36
NG_008156.2:g.42962A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4904A>G
ENST00000510728.6:n.1682A>G
ENST00000514776.3:n.127A>G
ENST00000515462.7:n.1881A>G
ENST00000626637.2:c.706A>G	ENSP00000486771.1:p.Arg236Gly
ENST00000638648.2:c.706A>G	ENSP00000507949.1:p.Arg236Gly
ENST00000640201.2:n.780A>G
ENST00000640752.2:n.4904A>G
ENST00000682067.1:c.527A>G
ENST00000682086.1:n.763A>G
ENST00000682373.1:c.353A>G
ENST00000684696.1:c.637-194A>G	ENSP00000507675.1:n.637-194A>G
ENST00000309522.8:c.694A>G MANE Select	ENSP00000312288.4:p.Arg232Gly
ENST00000403312.6:c.694A>G	ENSP00000385638.3:p.Arg232Gly
ENST00000505878.4:c.871A>G	ENSP00000425952.2:p.Arg291Gly
ENST00000514776.2:n.127A>G
ENST00000515462.6:n.1881A>G
ENST00000638559.1:c.552A>G
ENST00000638621.1:c.280A>G	ENSP00000491581.1:p.Arg94Gly
ENST00000638648.1:n.845A>G
ENST00000639146.1:c.694A>G	ENSP00000492345.1:p.Arg232Gly
ENST00000639335.1:c.*129A>G	ENSP00000491310.1:n.*129A>G
ENST00000639698.1:c.516+4182A>G	ENSP00000492420.1:n.516+4182A>G
ENST00000639784.1:c.373+4182A>G
ENST00000640048.1:c.666A>G	ENSP00000492009.1:n.666A>G
ENST00000640060.1:c.*789A>G	ENSP00000492734.1:n.*789A>G
ENST00000640201.1:n.649A>G
ENST00000640752.1:n.4897A>G
ENST00000309522.7:c.694A>G	ENSP00000312288.3:p.Arg232Gly
ENST00000403312.5:c.871A>G	ENSP00000385638.2:p.Arg291Gly
ENST00000505878.3:c.706A>G	ENSP00000425952.1:p.Arg236Gly
ENST00000507260.1:n.394A>G
ENST00000510728.5:n.234A>G
ENST00000515462.5:n.31A>G
ENST00000603302.5:c.694A>G	ENSP00000474560.1:p.Arg232Gly
ENST00000626637.1:c.706A>G	ENSP00000486771.1:p.Arg236Gly
NM_001184705.2:c.694A>G	NP_001171634.2:p.Arg232Gly
NM_005327.4:c.694A>G	NP_005318.3:p.Arg232Gly
XM_005262972.1:c.706A>G	XP_005263029.1:p.Arg236Gly
XR_938726.1:n.843A>G
NM_001331027.1:c.706A>G	NP_001317956.1:p.Arg236Gly
XR_001741214.2:n.788A>G
XR_002959727.1:n.788A>G
NM_001184705.3:c.694A>G	NP_001171634.2:p.Arg232Gly
NM_005327.7:c.694A>G MANE Select	NP_005318.6:p.Arg232Gly
NM_001184705.4:c.694A>G	NP_001171634.3:p.Arg232Gly
NM_001331027.2:c.706A>G	NP_001317956.2:p.Arg236Gly