Canonical Allele Identifier: CA1483969725
Gene: HADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108027947G= , CM000666.2:g.108027947G= GRCh38
NC_000004.11:g.108949103G= , CM000666.1:g.108949103G= GRCh37
NC_000004.10:g.109168552G= NCBI36
NG_008156.2:g.43164G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507260.3:n.5106G=
ENST00000510728.6:n.1706G=
ENST00000514776.3:n.329G=
ENST00000515462.7:n.2083G=
ENST00000626637.2:c.721+187G= ENSP00000486771.1:n.721+187G=
ENST00000638648.2:c.730G= ENSP00000507949.1:p.Gly244=
ENST00000640201.2:n.982G=
ENST00000640752.2:n.4919+187G=
ENST00000682067.1:c.542+187G=
ENST00000682086.1:n.965G=
ENST00000682373.1:c.368+187G=
ENST00000684696.1:c.645G= ENSP00000507675.1:p.Leu215=
ENST00000309522.8:c.709+187G= MANE Select ENSP00000312288.4:n.709+187G=
ENST00000403312.6:c.709+187G= ENSP00000385638.3:n.709+187G=
ENST00000505878.4:c.886+187G= ENSP00000425952.2:n.886+187G=
ENST00000514776.2:n.329G=
ENST00000515462.6:n.2083G=
ENST00000638559.1:c.567+187G=
ENST00000638621.1:c.295+187G= ENSP00000491581.1:n.295+187G=
ENST00000638648.1:n.860+187G=
ENST00000639146.1:c.718G= ENSP00000492345.1:p.Gly240=
ENST00000639335.1:c.*144+187G= ENSP00000491310.1:n.*144+187G=
ENST00000639698.1:c.516+4384G= ENSP00000492420.1:n.516+4384G=
ENST00000639784.1:c.373+4384G=
ENST00000640048.1:c.681+187G= ENSP00000492009.1:n.681+187G=
ENST00000640060.1:c.*804+187G= ENSP00000492734.1:n.*804+187G=
ENST00000640201.1:n.851G=
ENST00000640752.1:n.4912+187G=
ENST00000309522.7:c.709+187G= ENSP00000312288.3:n.709+187G=
ENST00000403312.5:c.886+187G= ENSP00000385638.2:n.886+187G=
ENST00000505878.3:c.721+187G= ENSP00000425952.1:n.721+187G=
ENST00000510728.5:n.258G=
ENST00000515462.5:n.233G=
ENST00000603302.5:c.709+187G= ENSP00000474560.1:n.709+187G=
ENST00000626637.1:c.721+187G= ENSP00000486771.1:n.721+187G=
NM_001184705.2:c.709+187G= NP_001171634.2:n.709+187G=
NM_005327.4:c.709+187G= NP_005318.3:n.709+187G=
XM_005262972.1:c.721+187G= XP_005263029.1:n.721+187G=
XR_938726.1:n.1045G=
NM_001331027.1:c.721+187G= NP_001317956.1:n.721+187G=
XR_001741214.2:n.812G=
XR_002959727.1:n.990G=
NM_001184705.3:c.709+187G= NP_001171634.2:n.709+187G=
NM_005327.7:c.709+187G= MANE Select NP_005318.6:n.709+187G=
NM_001184705.4:c.709+187G= NP_001171634.3:n.709+187G=
NM_001331027.2:c.721+187G= NP_001317956.2:n.721+187G=