Canonical Allele Identifier: CA357835708

Gene: HADH

Linked Data

• MyVariant Identifiers: chr4:g.108948843G>T (hg19) ; chr4:g.108027687G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027687G>T , CM000666.2:g.108027687G>T	GRCh38
NC_000004.11:g.108948843G>T , CM000666.1:g.108948843G>T	GRCh37
NC_000004.10:g.109168292G>T	NCBI36
NG_008156.2:g.42904G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4846G>T
ENST00000510728.6:n.1624G>T
ENST00000514776.3:n.69G>T
ENST00000515462.7:n.1823G>T
ENST00000626637.2:c.649-1G>T	ENSP00000486771.1:n.649-1G>T
ENST00000638648.2:c.649-1G>T	ENSP00000507949.1:n.649-1G>T
ENST00000640201.2:n.723-1G>T
ENST00000640752.2:n.4846G>T
ENST00000682067.1:c.470-1G>T
ENST00000682086.1:n.705G>T
ENST00000682373.1:c.296-1G>T
ENST00000684696.1:c.637-252G>T	ENSP00000507675.1:n.637-252G>T
ENST00000309522.8:c.637-1G>T MANE Select	ENSP00000312288.4:n.637-1G>T
ENST00000403312.6:c.637-1G>T	ENSP00000385638.3:n.637-1G>T
ENST00000505878.4:c.814-1G>T	ENSP00000425952.2:n.814-1G>T
ENST00000514776.2:n.69G>T
ENST00000515462.6:n.1823G>T
ENST00000638559.1:c.495-1G>T
ENST00000638621.1:c.223-1G>T	ENSP00000491581.1:n.223-1G>T
ENST00000638648.1:n.788-1G>T
ENST00000639146.1:c.637-1G>T	ENSP00000492345.1:n.637-1G>T
ENST00000639335.1:c.*72-1G>T	ENSP00000491310.1:n.*72-1G>T
ENST00000639698.1:c.516+4124G>T	ENSP00000492420.1:n.516+4124G>T
ENST00000639784.1:c.373+4124G>T
ENST00000640048.1:c.609-1G>T	ENSP00000492009.1:n.609-1G>T
ENST00000640060.1:c.*732-1G>T	ENSP00000492734.1:n.*732-1G>T
ENST00000640201.1:n.592-1G>T
ENST00000640752.1:n.4839G>T
ENST00000309522.7:c.637-1G>T	ENSP00000312288.3:n.637-1G>T
ENST00000403312.5:c.814-1G>T	ENSP00000385638.2:n.814-1G>T
ENST00000505878.3:c.649-1G>T	ENSP00000425952.1:n.649-1G>T
ENST00000507260.1:n.337-1G>T
ENST00000510728.5:n.176G>T
ENST00000603302.5:c.637-1G>T	ENSP00000474560.1:n.637-1G>T
ENST00000626637.1:c.649-1G>T	ENSP00000486771.1:n.649-1G>T
NM_001184705.2:c.637-1G>T	NP_001171634.2:n.637-1G>T
NM_005327.4:c.637-1G>T	NP_005318.3:n.637-1G>T
XM_005262972.1:c.649-1G>T	XP_005263029.1:n.649-1G>T
XR_938726.1:n.786-1G>T
NM_001331027.1:c.649-1G>T	NP_001317956.1:n.649-1G>T
XR_001741214.2:n.731-1G>T
XR_002959727.1:n.731-1G>T
NM_001184705.3:c.637-1G>T	NP_001171634.2:n.637-1G>T
NM_005327.7:c.637-1G>T MANE Select	NP_005318.6:n.637-1G>T
NM_001184705.4:c.637-1G>T	NP_001171634.3:n.637-1G>T
NM_001331027.2:c.649-1G>T	NP_001317956.2:n.649-1G>T