Canonical Allele Identifier: CA1483969309
Gene: HADH HGNC NCBI

Linked Data

dbSNP Id: rs1736110562

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108027678C>A , CM000666.2:g.108027678C>A GRCh38
NC_000004.11:g.108948834C>A , CM000666.1:g.108948834C>A GRCh37
NC_000004.10:g.109168283C>A NCBI36
NG_008156.2:g.42895C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000507260.3:n.4837C>A
ENST00000510728.6:n.1615C>A
ENST00000514776.3:n.60C>A
ENST00000515462.7:n.1814C>A
ENST00000626637.2:c.649-10C>A ENSP00000486771.1:n.649-10C>A
ENST00000638648.2:c.649-10C>A ENSP00000507949.1:n.649-10C>A
ENST00000640201.2:n.723-10C>A
ENST00000640752.2:n.4837C>A
ENST00000682067.1:c.470-10C>A
ENST00000682086.1:n.696C>A
ENST00000682373.1:c.296-10C>A
ENST00000684696.1:c.637-261C>A ENSP00000507675.1:n.637-261C>A
ENST00000309522.8:c.637-10C>A MANE Select ENSP00000312288.4:n.637-10C>A
ENST00000403312.6:c.637-10C>A ENSP00000385638.3:n.637-10C>A
ENST00000505878.4:c.814-10C>A ENSP00000425952.2:n.814-10C>A
ENST00000514776.2:n.60C>A
ENST00000515462.6:n.1814C>A
ENST00000638559.1:c.495-10C>A
ENST00000638621.1:c.223-10C>A ENSP00000491581.1:n.223-10C>A
ENST00000638648.1:n.788-10C>A
ENST00000639146.1:c.637-10C>A ENSP00000492345.1:n.637-10C>A
ENST00000639335.1:c.*72-10C>A ENSP00000491310.1:n.*72-10C>A
ENST00000639698.1:c.516+4115C>A ENSP00000492420.1:n.516+4115C>A
ENST00000639784.1:c.373+4115C>A
ENST00000640048.1:c.609-10C>A ENSP00000492009.1:n.609-10C>A
ENST00000640060.1:c.*732-10C>A ENSP00000492734.1:n.*732-10C>A
ENST00000640201.1:n.592-10C>A
ENST00000640752.1:n.4830C>A
ENST00000309522.7:c.637-10C>A ENSP00000312288.3:n.637-10C>A
ENST00000403312.5:c.814-10C>A ENSP00000385638.2:n.814-10C>A
ENST00000505878.3:c.649-10C>A ENSP00000425952.1:n.649-10C>A
ENST00000507260.1:n.337-10C>A
ENST00000510728.5:n.167C>A
ENST00000603302.5:c.637-10C>A ENSP00000474560.1:n.637-10C>A
ENST00000626637.1:c.649-10C>A ENSP00000486771.1:n.649-10C>A
NM_001184705.2:c.637-10C>A NP_001171634.2:n.637-10C>A
NM_005327.4:c.637-10C>A NP_005318.3:n.637-10C>A
XM_005262972.1:c.649-10C>A XP_005263029.1:n.649-10C>A
XR_938726.1:n.786-10C>A
NM_001331027.1:c.649-10C>A NP_001317956.1:n.649-10C>A
XR_001741214.2:n.731-10C>A
XR_002959727.1:n.731-10C>A
NM_001184705.3:c.637-10C>A NP_001171634.2:n.637-10C>A
NM_005327.7:c.637-10C>A MANE Select NP_005318.6:n.637-10C>A
NM_001184705.4:c.637-10C>A NP_001171634.3:n.637-10C>A
NM_001331027.2:c.649-10C>A NP_001317956.2:n.649-10C>A