Canonical Allele Identifier: CA10616855

Gene: HADH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.107989953G>A , CM000666.2:g.107989953G>A	GRCh38
NC_000004.11:g.108911109G>A , CM000666.1:g.108911109G>A	GRCh37
NC_000004.10:g.109130558G>A	NCBI36
NG_008156.2:g.5170G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005327.7:c.21G>A MANE Select	NP_005318.6:p.Gln7=
ENST00000309522.8:c.21G>A MANE Select	ENSP00000312288.4:p.Gln7=
NM_001184705.2:c.21G>A	NP_001171634.2:p.Gln7=
NM_001184705.3:c.21G>A	NP_001171634.2:p.Gln7=
NM_001184705.4:c.21G>A	NP_001171634.3:p.Gln7=
NM_005327.4:c.21G>A	NP_005318.3:p.Gln7=
ENST00000309522.7:c.21G>A	ENSP00000312288.3:p.Gln7=
ENST00000403312.5:c.198G>A	ENSP00000385638.2:p.Gln66=
ENST00000403312.6:c.21G>A	ENSP00000385638.3:p.Gln7=
ENST00000505878.3:c.-222G>A	ENSP00000425952.1:n.-222G>A
ENST00000505878.4:c.198G>A	ENSP00000425952.2:p.Gln66=
ENST00000507260.2:n.64G>A
ENST00000507260.3:n.107G>A
ENST00000511742.1:c.21G>A	ENSP00000425254.1:p.Gln7=
ENST00000603302.5:c.21G>A	ENSP00000474560.1:p.Gln7=
ENST00000638559.1:c.8G>A
ENST00000638621.1:c.21G>A	ENSP00000491581.1:p.Gln7=
ENST00000639013.1:n.96G>A
ENST00000639146.1:c.21G>A	ENSP00000492345.1:p.Gln7=
ENST00000639335.1:c.21G>A	ENSP00000491310.1:p.Gln7=
ENST00000640060.1:c.21G>A	ENSP00000492734.1:p.Gln7=
ENST00000640201.2:n.107G>A
ENST00000640752.1:n.100G>A
ENST00000640752.2:n.107G>A
ENST00000681992.1:n.58G>A
ENST00000682197.1:n.105G>A
ENST00000684696.1:c.21G>A	ENSP00000507675.1:p.Gln7=
XR_001741214.2:n.115G>A
XR_002959727.1:n.115G>A
XR_938726.1:n.170G>A