Canonical Allele Identifier: CA1483969657
Gene: HADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108027913T= , CM000666.2:g.108027913T= GRCh38
NC_000004.11:g.108949069T= , CM000666.1:g.108949069T= GRCh37
NC_000004.10:g.109168518T= NCBI36
NG_008156.2:g.43130T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507260.3:n.5072T=
ENST00000510728.6:n.1698-26T=
ENST00000514776.3:n.295T=
ENST00000515462.7:n.2049T=
ENST00000626637.2:c.721+153T= ENSP00000486771.1:n.721+153T=
ENST00000638648.2:c.722-26T= ENSP00000507949.1:n.722-26T=
ENST00000640201.2:n.948T=
ENST00000640752.2:n.4919+153T=
ENST00000682067.1:c.542+153T=
ENST00000682086.1:n.931T=
ENST00000682373.1:c.368+153T=
ENST00000684696.1:c.637-26T= ENSP00000507675.1:n.637-26T=
ENST00000309522.8:c.709+153T= MANE Select ENSP00000312288.4:n.709+153T=
ENST00000403312.6:c.709+153T= ENSP00000385638.3:n.709+153T=
ENST00000505878.4:c.886+153T= ENSP00000425952.2:n.886+153T=
ENST00000514776.2:n.295T=
ENST00000515462.6:n.2049T=
ENST00000638559.1:c.567+153T=
ENST00000638621.1:c.295+153T= ENSP00000491581.1:n.295+153T=
ENST00000638648.1:n.860+153T=
ENST00000639146.1:c.710-26T= ENSP00000492345.1:n.710-26T=
ENST00000639335.1:c.*144+153T= ENSP00000491310.1:n.*144+153T=
ENST00000639698.1:c.516+4350T= ENSP00000492420.1:n.516+4350T=
ENST00000639784.1:c.373+4350T=
ENST00000640048.1:c.681+153T= ENSP00000492009.1:n.681+153T=
ENST00000640060.1:c.*804+153T= ENSP00000492734.1:n.*804+153T=
ENST00000640201.1:n.817T=
ENST00000640752.1:n.4912+153T=
ENST00000309522.7:c.709+153T= ENSP00000312288.3:n.709+153T=
ENST00000403312.5:c.886+153T= ENSP00000385638.2:n.886+153T=
ENST00000505878.3:c.721+153T= ENSP00000425952.1:n.721+153T=
ENST00000507260.1:n.562T=
ENST00000510728.5:n.250-26T=
ENST00000515462.5:n.199T=
ENST00000603302.5:c.709+153T= ENSP00000474560.1:n.709+153T=
ENST00000626637.1:c.721+153T= ENSP00000486771.1:n.721+153T=
NM_001184705.2:c.709+153T= NP_001171634.2:n.709+153T=
NM_005327.4:c.709+153T= NP_005318.3:n.709+153T=
XM_005262972.1:c.721+153T= XP_005263029.1:n.721+153T=
XR_938726.1:n.1011T=
NM_001331027.1:c.721+153T= NP_001317956.1:n.721+153T=
XR_001741214.2:n.804-26T=
XR_002959727.1:n.956T=
NM_001184705.3:c.709+153T= NP_001171634.2:n.709+153T=
NM_005327.7:c.709+153T= MANE Select NP_005318.6:n.709+153T=
NM_001184705.4:c.709+153T= NP_001171634.3:n.709+153T=
NM_001331027.2:c.721+153T= NP_001317956.2:n.721+153T=