Canonical Allele Identifier: CA1483969779
Gene: HADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108027996C= , CM000666.2:g.108027996C= GRCh38
NC_000004.11:g.108949152C= , CM000666.1:g.108949152C= GRCh37
NC_000004.10:g.109168601C= NCBI36
NG_008156.2:g.43213C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507260.3:n.5155C=
ENST00000510728.6:n.1755C=
ENST00000514776.3:n.378C=
ENST00000515462.7:n.2132C=
ENST00000626637.2:c.721+236C= ENSP00000486771.1:n.721+236C=
ENST00000638648.2:c.*29C= ENSP00000507949.1:n.*29C=
ENST00000640201.2:n.1031C=
ENST00000640752.2:n.4919+236C=
ENST00000682067.1:c.542+236C=
ENST00000682086.1:n.1014C=
ENST00000682373.1:c.368+236C=
ENST00000684696.1:c.694C= ENSP00000507675.1:p.His232=
ENST00000309522.8:c.709+236C= MANE Select ENSP00000312288.4:n.709+236C=
ENST00000403312.6:c.709+236C= ENSP00000385638.3:n.709+236C=
ENST00000505878.4:c.886+236C= ENSP00000425952.2:n.886+236C=
ENST00000514776.2:n.378C=
ENST00000515462.6:n.2132C=
ENST00000638559.1:c.567+236C=
ENST00000638621.1:c.295+236C= ENSP00000491581.1:n.295+236C=
ENST00000638648.1:n.860+236C=
ENST00000639146.1:c.*29C= ENSP00000492345.1:n.*29C=
ENST00000639335.1:c.*144+236C= ENSP00000491310.1:n.*144+236C=
ENST00000639698.1:c.516+4433C= ENSP00000492420.1:n.516+4433C=
ENST00000639784.1:c.373+4433C=
ENST00000640048.1:c.681+236C= ENSP00000492009.1:n.681+236C=
ENST00000640060.1:c.*804+236C= ENSP00000492734.1:n.*804+236C=
ENST00000640201.1:n.900C=
ENST00000640752.1:n.4912+236C=
ENST00000309522.7:c.709+236C= ENSP00000312288.3:n.709+236C=
ENST00000403312.5:c.886+236C= ENSP00000385638.2:n.886+236C=
ENST00000505878.3:c.721+236C= ENSP00000425952.1:n.721+236C=
ENST00000510728.5:n.307C=
ENST00000515462.5:n.282C=
ENST00000603302.5:c.709+236C= ENSP00000474560.1:n.709+236C=
ENST00000626637.1:c.721+236C= ENSP00000486771.1:n.721+236C=
NM_001184705.2:c.709+236C= NP_001171634.2:n.709+236C=
NM_005327.4:c.709+236C= NP_005318.3:n.709+236C=
XM_005262972.1:c.721+236C= XP_005263029.1:n.721+236C=
XR_938726.1:n.1094C=
NM_001331027.1:c.721+236C= NP_001317956.1:n.721+236C=
XR_001741214.2:n.861C=
XR_002959727.1:n.1039C=
NM_001184705.3:c.709+236C= NP_001171634.2:n.709+236C=
NM_005327.7:c.709+236C= MANE Select NP_005318.6:n.709+236C=
NM_001184705.4:c.709+236C= NP_001171634.3:n.709+236C=
NM_001331027.2:c.721+236C= NP_001317956.2:n.721+236C=