Canonical Allele Identifier: CA440568458

Gene: HADH

Linked Data

• MyVariant Identifiers: chr4:g.108948879T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027723T>C , CM000666.2:g.108027723T>C	GRCh38
NC_000004.11:g.108948879T>C , CM000666.1:g.108948879T>C	GRCh37
NC_000004.10:g.109168328T>C	NCBI36
NG_008156.2:g.42940T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4882T>C
ENST00000510728.6:n.1660T>C
ENST00000514776.3:n.105T>C
ENST00000515462.7:n.1859T>C
ENST00000626637.2:c.684T>C	ENSP00000486771.1:p.Val228=
ENST00000638648.2:c.684T>C	ENSP00000507949.1:p.Val228=
ENST00000640201.2:n.758T>C
ENST00000640752.2:n.4882T>C
ENST00000682067.1:c.505T>C
ENST00000682086.1:n.741T>C
ENST00000682373.1:c.331T>C
ENST00000684696.1:c.637-216T>C	ENSP00000507675.1:n.637-216T>C
ENST00000309522.8:c.672T>C MANE Select	ENSP00000312288.4:p.Val224=
ENST00000403312.6:c.672T>C	ENSP00000385638.3:p.Val224=
ENST00000505878.4:c.849T>C	ENSP00000425952.2:p.Val283=
ENST00000514776.2:n.105T>C
ENST00000515462.6:n.1859T>C
ENST00000638559.1:c.530T>C
ENST00000638621.1:c.258T>C	ENSP00000491581.1:p.Val86=
ENST00000638648.1:n.823T>C
ENST00000639146.1:c.672T>C	ENSP00000492345.1:p.Val224=
ENST00000639335.1:c.*107T>C	ENSP00000491310.1:n.*107T>C
ENST00000639698.1:c.516+4160T>C	ENSP00000492420.1:n.516+4160T>C
ENST00000639784.1:c.373+4160T>C
ENST00000640048.1:c.644T>C	ENSP00000492009.1:n.644T>C
ENST00000640060.1:c.*767T>C	ENSP00000492734.1:n.*767T>C
ENST00000640201.1:n.627T>C
ENST00000640752.1:n.4875T>C
ENST00000309522.7:c.672T>C	ENSP00000312288.3:p.Val224=
ENST00000403312.5:c.849T>C	ENSP00000385638.2:p.Val283=
ENST00000505878.3:c.684T>C	ENSP00000425952.1:p.Val228=
ENST00000507260.1:n.372T>C
ENST00000510728.5:n.212T>C
ENST00000515462.5:n.9T>C
ENST00000603302.5:c.672T>C	ENSP00000474560.1:p.Val224=
ENST00000626637.1:c.684T>C	ENSP00000486771.1:p.Val228=
NM_001184705.2:c.672T>C	NP_001171634.2:p.Val224=
NM_005327.4:c.672T>C	NP_005318.3:p.Val224=
XM_005262972.1:c.684T>C	XP_005263029.1:p.Val228=
XR_938726.1:n.821T>C
NM_001331027.1:c.684T>C	NP_001317956.1:p.Val228=
XR_001741214.2:n.766T>C
XR_002959727.1:n.766T>C
NM_001184705.3:c.672T>C	NP_001171634.2:p.Val224=
NM_005327.7:c.672T>C MANE Select	NP_005318.6:p.Val224=
NM_001184705.4:c.672T>C	NP_001171634.3:p.Val224=
NM_001331027.2:c.684T>C	NP_001317956.2:p.Val228=