Canonical Allele Identifier: CA357835734

Gene: HADH

Linked Data

• MyVariant Identifiers: chr4:g.108948847A>C (hg19) ; chr4:g.108027691A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027691A>C , CM000666.2:g.108027691A>C	GRCh38
NC_000004.11:g.108948847A>C , CM000666.1:g.108948847A>C	GRCh37
NC_000004.10:g.109168296A>C	NCBI36
NG_008156.2:g.42908A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4850A>C
ENST00000510728.6:n.1628A>C
ENST00000514776.3:n.73A>C
ENST00000515462.7:n.1827A>C
ENST00000626637.2:c.652A>C	ENSP00000486771.1:p.Thr218Pro
ENST00000638648.2:c.652A>C	ENSP00000507949.1:p.Thr218Pro
ENST00000640201.2:n.726A>C
ENST00000640752.2:n.4850A>C
ENST00000682067.1:c.473A>C
ENST00000682086.1:n.709A>C
ENST00000682373.1:c.299A>C
ENST00000684696.1:c.637-248A>C	ENSP00000507675.1:n.637-248A>C
ENST00000309522.8:c.640A>C MANE Select	ENSP00000312288.4:p.Thr214Pro
ENST00000403312.6:c.640A>C	ENSP00000385638.3:p.Thr214Pro
ENST00000505878.4:c.817A>C	ENSP00000425952.2:p.Thr273Pro
ENST00000514776.2:n.73A>C
ENST00000515462.6:n.1827A>C
ENST00000638559.1:c.498A>C
ENST00000638621.1:c.226A>C	ENSP00000491581.1:p.Thr76Pro
ENST00000638648.1:n.791A>C
ENST00000639146.1:c.640A>C	ENSP00000492345.1:p.Thr214Pro
ENST00000639335.1:c.*75A>C	ENSP00000491310.1:n.*75A>C
ENST00000639698.1:c.516+4128A>C	ENSP00000492420.1:n.516+4128A>C
ENST00000639784.1:c.373+4128A>C
ENST00000640048.1:c.612A>C	ENSP00000492009.1:n.612A>C
ENST00000640060.1:c.*735A>C	ENSP00000492734.1:n.*735A>C
ENST00000640201.1:n.595A>C
ENST00000640752.1:n.4843A>C
ENST00000309522.7:c.640A>C	ENSP00000312288.3:p.Thr214Pro
ENST00000403312.5:c.817A>C	ENSP00000385638.2:p.Thr273Pro
ENST00000505878.3:c.652A>C	ENSP00000425952.1:p.Thr218Pro
ENST00000507260.1:n.340A>C
ENST00000510728.5:n.180A>C
ENST00000603302.5:c.640A>C	ENSP00000474560.1:p.Thr214Pro
ENST00000626637.1:c.652A>C	ENSP00000486771.1:p.Thr218Pro
NM_001184705.2:c.640A>C	NP_001171634.2:p.Thr214Pro
NM_005327.4:c.640A>C	NP_005318.3:p.Thr214Pro
XM_005262972.1:c.652A>C	XP_005263029.1:p.Thr218Pro
XR_938726.1:n.789A>C
NM_001331027.1:c.652A>C	NP_001317956.1:p.Thr218Pro
XR_001741214.2:n.734A>C
XR_002959727.1:n.734A>C
NM_001184705.3:c.640A>C	NP_001171634.2:p.Thr214Pro
NM_005327.7:c.640A>C MANE Select	NP_005318.6:p.Thr214Pro
NM_001184705.4:c.640A>C	NP_001171634.3:p.Thr214Pro
NM_001331027.2:c.652A>C	NP_001317956.2:p.Thr218Pro