Canonical Allele Identifier: CA102861968

Gene: HADH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108034525A>T , CM000666.2:g.108034525A>T	GRCh38
NC_000004.11:g.108955681A>T , CM000666.1:g.108955681A>T	GRCh37
NC_000004.10:g.109175130A>T	NCBI36
NG_008156.2:g.49742A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005327.7:c.*168A>T MANE Select	NP_005318.6:n.*168A>T
ENST00000309522.8:c.*168A>T MANE Select	ENSP00000312288.4:n.*168A>T
NM_001184705.2:c.*168A>T	NP_001171634.2:n.*168A>T
NM_001184705.3:c.*168A>T	NP_001171634.2:n.*168A>T
NM_001184705.4:c.*168A>T	NP_001171634.3:n.*168A>T
NM_001331027.1:c.*168A>T	NP_001317956.1:n.*168A>T
NM_001331027.2:c.*168A>T	NP_001317956.2:n.*168A>T
NM_005327.4:c.*168A>T	NP_005318.3:n.*168A>T
ENST00000309522.7:c.*168A>T	ENSP00000312288.3:n.*168A>T
ENST00000403312.5:c.*168A>T	ENSP00000385638.2:n.*168A>T
ENST00000403312.6:c.*168A>T	ENSP00000385638.3:n.*168A>T
ENST00000505878.3:c.*168A>T	ENSP00000425952.1:n.*168A>T
ENST00000505878.4:c.*168A>T	ENSP00000425952.2:n.*168A>T
ENST00000507260.3:n.5632A>T
ENST00000510728.6:n.2232A>T
ENST00000514776.2:n.5961A>T
ENST00000514776.3:n.5961A>T
ENST00000515462.6:n.2609A>T
ENST00000515462.7:n.2609A>T
ENST00000603302.5:c.*168A>T	ENSP00000474560.1:n.*168A>T
ENST00000626637.1:c.1125A>T	ENSP00000486771.1:n.1125A>T
ENST00000626637.2:c.*168A>T	ENSP00000486771.1:n.*168A>T
ENST00000638559.1:c.971A>T
ENST00000638648.1:n.1264A>T
ENST00000638648.2:c.*506A>T	ENSP00000507949.1:n.*506A>T
ENST00000639146.1:c.*506A>T	ENSP00000492345.1:n.*506A>T
ENST00000639335.1:c.*548A>T	ENSP00000491310.1:n.*548A>T
ENST00000639698.1:c.920A>T	ENSP00000492420.1:n.920A>T
ENST00000639784.1:c.777A>T
ENST00000640048.1:c.1085A>T	ENSP00000492009.1:n.1085A>T
ENST00000640060.1:c.*1208A>T	ENSP00000492734.1:n.*1208A>T
ENST00000640201.1:n.1377A>T
ENST00000640201.2:n.1508A>T
ENST00000640752.1:n.5316A>T
ENST00000640752.2:n.5323A>T
ENST00000682067.1:c.660-70A>T
ENST00000682086.1:n.1406-70A>T
ENST00000682373.1:c.772A>T
ENST00000684696.1:c.*433A>T	ENSP00000507675.1:n.*433A>T
XM_005262972.1:c.*168A>T	XP_005263029.1:n.*168A>T
XR_001741214.2:n.1338A>T
XR_002959727.1:n.1516A>T
XR_938726.1:n.1571A>T