Canonical Allele Identifier: CA357835977

Gene: HADH

Linked Data

• MyVariant Identifiers: chr4:g.108948895G>T (hg19) ; chr4:g.108027739G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027739G>T , CM000666.2:g.108027739G>T	GRCh38
NC_000004.11:g.108948895G>T , CM000666.1:g.108948895G>T	GRCh37
NC_000004.10:g.109168344G>T	NCBI36
NG_008156.2:g.42956G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4898G>T
ENST00000510728.6:n.1676G>T
ENST00000514776.3:n.121G>T
ENST00000515462.7:n.1875G>T
ENST00000626637.2:c.700G>T	ENSP00000486771.1:p.Ala234Ser
ENST00000638648.2:c.700G>T	ENSP00000507949.1:p.Ala234Ser
ENST00000640201.2:n.774G>T
ENST00000640752.2:n.4898G>T
ENST00000682067.1:c.521G>T
ENST00000682086.1:n.757G>T
ENST00000682373.1:c.347G>T
ENST00000684696.1:c.637-200G>T	ENSP00000507675.1:n.637-200G>T
ENST00000309522.8:c.688G>T MANE Select	ENSP00000312288.4:p.Ala230Ser
ENST00000403312.6:c.688G>T	ENSP00000385638.3:p.Ala230Ser
ENST00000505878.4:c.865G>T	ENSP00000425952.2:p.Ala289Ser
ENST00000514776.2:n.121G>T
ENST00000515462.6:n.1875G>T
ENST00000638559.1:c.546G>T
ENST00000638621.1:c.274G>T	ENSP00000491581.1:p.Ala92Ser
ENST00000638648.1:n.839G>T
ENST00000639146.1:c.688G>T	ENSP00000492345.1:p.Ala230Ser
ENST00000639335.1:c.*123G>T	ENSP00000491310.1:n.*123G>T
ENST00000639698.1:c.516+4176G>T	ENSP00000492420.1:n.516+4176G>T
ENST00000639784.1:c.373+4176G>T
ENST00000640048.1:c.660G>T	ENSP00000492009.1:n.660G>T
ENST00000640060.1:c.*783G>T	ENSP00000492734.1:n.*783G>T
ENST00000640201.1:n.643G>T
ENST00000640752.1:n.4891G>T
ENST00000309522.7:c.688G>T	ENSP00000312288.3:p.Ala230Ser
ENST00000403312.5:c.865G>T	ENSP00000385638.2:p.Ala289Ser
ENST00000505878.3:c.700G>T	ENSP00000425952.1:p.Ala234Ser
ENST00000507260.1:n.388G>T
ENST00000510728.5:n.228G>T
ENST00000515462.5:n.25G>T
ENST00000603302.5:c.688G>T	ENSP00000474560.1:p.Ala230Ser
ENST00000626637.1:c.700G>T	ENSP00000486771.1:p.Ala234Ser
NM_001184705.2:c.688G>T	NP_001171634.2:p.Ala230Ser
NM_005327.4:c.688G>T	NP_005318.3:p.Ala230Ser
XM_005262972.1:c.700G>T	XP_005263029.1:p.Ala234Ser
XR_938726.1:n.837G>T
NM_001331027.1:c.700G>T	NP_001317956.1:p.Ala234Ser
XR_001741214.2:n.782G>T
XR_002959727.1:n.782G>T
NM_001184705.3:c.688G>T	NP_001171634.2:p.Ala230Ser
NM_005327.7:c.688G>T MANE Select	NP_005318.6:p.Ala230Ser
NM_001184705.4:c.688G>T	NP_001171634.3:p.Ala230Ser
NM_001331027.2:c.700G>T	NP_001317956.2:p.Ala234Ser