Canonical Allele Identifier: CA1483969501

Gene: HADH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027792_108027793delinsAC , CM000666.2:g.108027792_108027793delinsAC	GRCh38
NC_000004.11:g.108948948_108948949delinsAC , CM000666.1:g.108948948_108948949delinsAC	GRCh37
NC_000004.10:g.109168397_109168398delinsAC	NCBI36
NG_008156.2:g.43009_43010delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4951_4952delinsAC
ENST00000510728.6:n.1697+32_1697+33delinsAC
ENST00000514776.3:n.174_175delinsAC
ENST00000515462.7:n.1928_1929delinsAC
ENST00000626637.2:c.721+32_721+33delinsAC	ENSP00000486771.1:n.721+32_721+33delinsAC
ENST00000638648.2:c.721+32_721+33delinsAC	ENSP00000507949.1:n.721+32_721+33delinsAC
ENST00000640201.2:n.827_828delinsAC
ENST00000640752.2:n.4919+32_4919+33delinsAC
ENST00000682067.1:c.542+32_542+33delinsAC
ENST00000682086.1:n.810_811delinsAC
ENST00000682373.1:c.368+32_368+33delinsAC
ENST00000684696.1:c.637-147_637-146delinsAC	ENSP00000507675.1:n.637-147_637-146delinsAC
ENST00000309522.8:c.709+32_709+33delinsAC MANE Select	ENSP00000312288.4:n.709+32_709+33delinsAC
ENST00000403312.6:c.709+32_709+33delinsAC	ENSP00000385638.3:n.709+32_709+33delinsAC
ENST00000505878.4:c.886+32_886+33delinsAC	ENSP00000425952.2:n.886+32_886+33delinsAC
ENST00000514776.2:n.174_175delinsAC
ENST00000515462.6:n.1928_1929delinsAC
ENST00000638559.1:c.567+32_567+33delinsAC
ENST00000638621.1:c.295+32_295+33delinsAC	ENSP00000491581.1:n.295+32_295+33delinsAC
ENST00000638648.1:n.860+32_860+33delinsAC
ENST00000639146.1:c.709+32_709+33delinsAC	ENSP00000492345.1:n.709+32_709+33delinsAC
ENST00000639335.1:c.*144+32_*144+33delinsAC	ENSP00000491310.1:n.*144+32_*144+33delinsAC
ENST00000639698.1:c.516+4229_516+4230delinsAC	ENSP00000492420.1:n.516+4229_516+4230delinsAC
ENST00000639784.1:c.373+4229_373+4230delinsAC
ENST00000640048.1:c.681+32_681+33delinsAC	ENSP00000492009.1:n.681+32_681+33delinsAC
ENST00000640060.1:c.*804+32_*804+33delinsAC	ENSP00000492734.1:n.*804+32_*804+33delinsAC
ENST00000640201.1:n.696_697delinsAC
ENST00000640752.1:n.4912+32_4912+33delinsAC
ENST00000309522.7:c.709+32_709+33delinsAC	ENSP00000312288.3:n.709+32_709+33delinsAC
ENST00000403312.5:c.886+32_886+33delinsAC	ENSP00000385638.2:n.886+32_886+33delinsAC
ENST00000505878.3:c.721+32_721+33delinsAC	ENSP00000425952.1:n.721+32_721+33delinsAC
ENST00000507260.1:n.441_442delinsAC
ENST00000510728.5:n.249+32_249+33delinsAC
ENST00000515462.5:n.78_79delinsAC
ENST00000603302.5:c.709+32_709+33delinsAC	ENSP00000474560.1:n.709+32_709+33delinsAC
ENST00000626637.1:c.721+32_721+33delinsAC	ENSP00000486771.1:n.721+32_721+33delinsAC
NM_001184705.2:c.709+32_709+33delinsAC	NP_001171634.2:n.709+32_709+33delinsAC
NM_005327.4:c.709+32_709+33delinsAC	NP_005318.3:n.709+32_709+33delinsAC
XM_005262972.1:c.721+32_721+33delinsAC	XP_005263029.1:n.721+32_721+33delinsAC
XR_938726.1:n.890_891delinsAC
NM_001331027.1:c.721+32_721+33delinsAC	NP_001317956.1:n.721+32_721+33delinsAC
XR_001741214.2:n.803+32_803+33delinsAC
XR_002959727.1:n.835_836delinsAC
NM_001184705.3:c.709+32_709+33delinsAC	NP_001171634.2:n.709+32_709+33delinsAC
NM_005327.7:c.709+32_709+33delinsAC MANE Select	NP_005318.6:n.709+32_709+33delinsAC
NM_001184705.4:c.709+32_709+33delinsAC	NP_001171634.3:n.709+32_709+33delinsAC
NM_001331027.2:c.721+32_721+33delinsAC	NP_001317956.2:n.721+32_721+33delinsAC