Canonical Allele Identifier: CA1483969355
Gene: HADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108027712C= , CM000666.2:g.108027712C= GRCh38
NC_000004.11:g.108948868C= , CM000666.1:g.108948868C= GRCh37
NC_000004.10:g.109168317C= NCBI36
NG_008156.2:g.42929C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507260.3:n.4871C=
ENST00000510728.6:n.1649C=
ENST00000514776.3:n.94C=
ENST00000515462.7:n.1848C=
ENST00000626637.2:c.673C= ENSP00000486771.1:p.Arg225=
ENST00000638648.2:c.673C= ENSP00000507949.1:p.Arg225=
ENST00000640201.2:n.747C=
ENST00000640752.2:n.4871C=
ENST00000682067.1:c.494C=
ENST00000682086.1:n.730C=
ENST00000682373.1:c.320C=
ENST00000684696.1:c.637-227C= ENSP00000507675.1:n.637-227C=
ENST00000309522.8:c.661C= MANE Select ENSP00000312288.4:p.Arg221=
ENST00000403312.6:c.661C= ENSP00000385638.3:p.Arg221=
ENST00000505878.4:c.838C= ENSP00000425952.2:p.Arg280=
ENST00000514776.2:n.94C=
ENST00000515462.6:n.1848C=
ENST00000638559.1:c.519C=
ENST00000638621.1:c.247C= ENSP00000491581.1:p.Arg83=
ENST00000638648.1:n.812C=
ENST00000639146.1:c.661C= ENSP00000492345.1:p.Arg221=
ENST00000639335.1:c.*96C= ENSP00000491310.1:n.*96C=
ENST00000639698.1:c.516+4149C= ENSP00000492420.1:n.516+4149C=
ENST00000639784.1:c.373+4149C=
ENST00000640048.1:c.633C= ENSP00000492009.1:n.633C=
ENST00000640060.1:c.*756C= ENSP00000492734.1:n.*756C=
ENST00000640201.1:n.616C=
ENST00000640752.1:n.4864C=
ENST00000309522.7:c.661C= ENSP00000312288.3:p.Arg221=
ENST00000403312.5:c.838C= ENSP00000385638.2:p.Arg280=
ENST00000505878.3:c.673C= ENSP00000425952.1:p.Arg225=
ENST00000507260.1:n.361C=
ENST00000510728.5:n.201C=
ENST00000603302.5:c.661C= ENSP00000474560.1:p.Arg221=
ENST00000626637.1:c.673C= ENSP00000486771.1:p.Arg225=
NM_001184705.2:c.661C= NP_001171634.2:p.Arg221=
NM_005327.4:c.661C= NP_005318.3:p.Arg221=
XM_005262972.1:c.673C= XP_005263029.1:p.Arg225=
XR_938726.1:n.810C=
NM_001331027.1:c.673C= NP_001317956.1:p.Arg225=
XR_001741214.2:n.755C=
XR_002959727.1:n.755C=
NM_001184705.3:c.661C= NP_001171634.2:p.Arg221=
NM_005327.7:c.661C= MANE Select NP_005318.6:p.Arg221=
NM_001184705.4:c.661C= NP_001171634.3:p.Arg221=
NM_001331027.2:c.673C= NP_001317956.2:p.Arg225=