Canonical Allele Identifier: CA1483969649
Gene: HADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108027907G= , CM000666.2:g.108027907G= GRCh38
NC_000004.11:g.108949063G= , CM000666.1:g.108949063G= GRCh37
NC_000004.10:g.109168512G= NCBI36
NG_008156.2:g.43124G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507260.3:n.5066G=
ENST00000510728.6:n.1698-32G=
ENST00000514776.3:n.289G=
ENST00000515462.7:n.2043G=
ENST00000626637.2:c.721+147G= ENSP00000486771.1:n.721+147G=
ENST00000638648.2:c.722-32G= ENSP00000507949.1:n.722-32G=
ENST00000640201.2:n.942G=
ENST00000640752.2:n.4919+147G=
ENST00000682067.1:c.542+147G=
ENST00000682086.1:n.925G=
ENST00000682373.1:c.368+147G=
ENST00000684696.1:c.637-32G= ENSP00000507675.1:n.637-32G=
ENST00000309522.8:c.709+147G= MANE Select ENSP00000312288.4:n.709+147G=
ENST00000403312.6:c.709+147G= ENSP00000385638.3:n.709+147G=
ENST00000505878.4:c.886+147G= ENSP00000425952.2:n.886+147G=
ENST00000514776.2:n.289G=
ENST00000515462.6:n.2043G=
ENST00000638559.1:c.567+147G=
ENST00000638621.1:c.295+147G= ENSP00000491581.1:n.295+147G=
ENST00000638648.1:n.860+147G=
ENST00000639146.1:c.710-32G= ENSP00000492345.1:n.710-32G=
ENST00000639335.1:c.*144+147G= ENSP00000491310.1:n.*144+147G=
ENST00000639698.1:c.516+4344G= ENSP00000492420.1:n.516+4344G=
ENST00000639784.1:c.373+4344G=
ENST00000640048.1:c.681+147G= ENSP00000492009.1:n.681+147G=
ENST00000640060.1:c.*804+147G= ENSP00000492734.1:n.*804+147G=
ENST00000640201.1:n.811G=
ENST00000640752.1:n.4912+147G=
ENST00000309522.7:c.709+147G= ENSP00000312288.3:n.709+147G=
ENST00000403312.5:c.886+147G= ENSP00000385638.2:n.886+147G=
ENST00000505878.3:c.721+147G= ENSP00000425952.1:n.721+147G=
ENST00000507260.1:n.556G=
ENST00000510728.5:n.250-32G=
ENST00000515462.5:n.193G=
ENST00000603302.5:c.709+147G= ENSP00000474560.1:n.709+147G=
ENST00000626637.1:c.721+147G= ENSP00000486771.1:n.721+147G=
NM_001184705.2:c.709+147G= NP_001171634.2:n.709+147G=
NM_005327.4:c.709+147G= NP_005318.3:n.709+147G=
XM_005262972.1:c.721+147G= XP_005263029.1:n.721+147G=
XR_938726.1:n.1005G=
NM_001331027.1:c.721+147G= NP_001317956.1:n.721+147G=
XR_001741214.2:n.804-32G=
XR_002959727.1:n.950G=
NM_001184705.3:c.709+147G= NP_001171634.2:n.709+147G=
NM_005327.7:c.709+147G= MANE Select NP_005318.6:n.709+147G=
NM_001184705.4:c.709+147G= NP_001171634.3:n.709+147G=
NM_001331027.2:c.721+147G= NP_001317956.2:n.721+147G=