Canonical Allele Identifier: CA1483969744

Gene: HADH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027971A= , CM000666.2:g.108027971A=	GRCh38
NC_000004.11:g.108949127A= , CM000666.1:g.108949127A=	GRCh37
NC_000004.10:g.109168576A=	NCBI36
NG_008156.2:g.43188A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.5130A=
ENST00000510728.6:n.1730A=
ENST00000514776.3:n.353A=
ENST00000515462.7:n.2107A=
ENST00000626637.2:c.721+211A=	ENSP00000486771.1:n.721+211A=
ENST00000638648.2:c.*4A=	ENSP00000507949.1:n.*4A=
ENST00000640201.2:n.1006A=
ENST00000640752.2:n.4919+211A=
ENST00000682067.1:c.542+211A=
ENST00000682086.1:n.989A=
ENST00000682373.1:c.368+211A=
ENST00000684696.1:c.669A=	ENSP00000507675.1:p.Lys223=
ENST00000309522.8:c.709+211A= MANE Select	ENSP00000312288.4:n.709+211A=
ENST00000403312.6:c.709+211A=	ENSP00000385638.3:n.709+211A=
ENST00000505878.4:c.886+211A=	ENSP00000425952.2:n.886+211A=
ENST00000514776.2:n.353A=
ENST00000515462.6:n.2107A=
ENST00000638559.1:c.567+211A=
ENST00000638621.1:c.295+211A=	ENSP00000491581.1:n.295+211A=
ENST00000638648.1:n.860+211A=
ENST00000639146.1:c.*4A=	ENSP00000492345.1:n.*4A=
ENST00000639335.1:c.*144+211A=	ENSP00000491310.1:n.*144+211A=
ENST00000639698.1:c.516+4408A=	ENSP00000492420.1:n.516+4408A=
ENST00000639784.1:c.373+4408A=
ENST00000640048.1:c.681+211A=	ENSP00000492009.1:n.681+211A=
ENST00000640060.1:c.*804+211A=	ENSP00000492734.1:n.*804+211A=
ENST00000640201.1:n.875A=
ENST00000640752.1:n.4912+211A=
ENST00000309522.7:c.709+211A=	ENSP00000312288.3:n.709+211A=
ENST00000403312.5:c.886+211A=	ENSP00000385638.2:n.886+211A=
ENST00000505878.3:c.721+211A=	ENSP00000425952.1:n.721+211A=
ENST00000510728.5:n.282A=
ENST00000515462.5:n.257A=
ENST00000603302.5:c.709+211A=	ENSP00000474560.1:n.709+211A=
ENST00000626637.1:c.721+211A=	ENSP00000486771.1:n.721+211A=
NM_001184705.2:c.709+211A=	NP_001171634.2:n.709+211A=
NM_005327.4:c.709+211A=	NP_005318.3:n.709+211A=
XM_005262972.1:c.721+211A=	XP_005263029.1:n.721+211A=
XR_938726.1:n.1069A=
NM_001331027.1:c.721+211A=	NP_001317956.1:n.721+211A=
XR_001741214.2:n.836A=
XR_002959727.1:n.1014A=
NM_001184705.3:c.709+211A=	NP_001171634.2:n.709+211A=
NM_005327.7:c.709+211A= MANE Select	NP_005318.6:n.709+211A=
NM_001184705.4:c.709+211A=	NP_001171634.3:n.709+211A=
NM_001331027.2:c.721+211A=	NP_001317956.2:n.721+211A=