Canonical Allele Identifier: CA357835993

Gene: HADH

Linked Data

• MyVariant Identifiers: chr4:g.108948899T>C (hg19) ; chr4:g.108027743T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027743T>C , CM000666.2:g.108027743T>C	GRCh38
NC_000004.11:g.108948899T>C , CM000666.1:g.108948899T>C	GRCh37
NC_000004.10:g.109168348T>C	NCBI36
NG_008156.2:g.42960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4902T>C
ENST00000510728.6:n.1680T>C
ENST00000514776.3:n.125T>C
ENST00000515462.7:n.1879T>C
ENST00000626637.2:c.704T>C	ENSP00000486771.1:p.Ile235Thr
ENST00000638648.2:c.704T>C	ENSP00000507949.1:p.Ile235Thr
ENST00000640201.2:n.778T>C
ENST00000640752.2:n.4902T>C
ENST00000682067.1:c.525T>C
ENST00000682086.1:n.761T>C
ENST00000682373.1:c.351T>C
ENST00000684696.1:c.637-196T>C	ENSP00000507675.1:n.637-196T>C
ENST00000309522.8:c.692T>C MANE Select	ENSP00000312288.4:p.Ile231Thr
ENST00000403312.6:c.692T>C	ENSP00000385638.3:p.Ile231Thr
ENST00000505878.4:c.869T>C	ENSP00000425952.2:p.Ile290Thr
ENST00000514776.2:n.125T>C
ENST00000515462.6:n.1879T>C
ENST00000638559.1:c.550T>C
ENST00000638621.1:c.278T>C	ENSP00000491581.1:p.Ile93Thr
ENST00000638648.1:n.843T>C
ENST00000639146.1:c.692T>C	ENSP00000492345.1:p.Ile231Thr
ENST00000639335.1:c.*127T>C	ENSP00000491310.1:n.*127T>C
ENST00000639698.1:c.516+4180T>C	ENSP00000492420.1:n.516+4180T>C
ENST00000639784.1:c.373+4180T>C
ENST00000640048.1:c.664T>C	ENSP00000492009.1:n.664T>C
ENST00000640060.1:c.*787T>C	ENSP00000492734.1:n.*787T>C
ENST00000640201.1:n.647T>C
ENST00000640752.1:n.4895T>C
ENST00000309522.7:c.692T>C	ENSP00000312288.3:p.Ile231Thr
ENST00000403312.5:c.869T>C	ENSP00000385638.2:p.Ile290Thr
ENST00000505878.3:c.704T>C	ENSP00000425952.1:p.Ile235Thr
ENST00000507260.1:n.392T>C
ENST00000510728.5:n.232T>C
ENST00000515462.5:n.29T>C
ENST00000603302.5:c.692T>C	ENSP00000474560.1:p.Ile231Thr
ENST00000626637.1:c.704T>C	ENSP00000486771.1:p.Ile235Thr
NM_001184705.2:c.692T>C	NP_001171634.2:p.Ile231Thr
NM_005327.4:c.692T>C	NP_005318.3:p.Ile231Thr
XM_005262972.1:c.704T>C	XP_005263029.1:p.Ile235Thr
XR_938726.1:n.841T>C
NM_001331027.1:c.704T>C	NP_001317956.1:p.Ile235Thr
XR_001741214.2:n.786T>C
XR_002959727.1:n.786T>C
NM_001184705.3:c.692T>C	NP_001171634.2:p.Ile231Thr
NM_005327.7:c.692T>C MANE Select	NP_005318.6:p.Ile231Thr
NM_001184705.4:c.692T>C	NP_001171634.3:p.Ile231Thr
NM_001331027.2:c.704T>C	NP_001317956.2:p.Ile235Thr