Canonical Allele Identifier: CA3037545
Community Standard Title: NM_005327.7(HADH):c.662G>A (p.Arg221His)
Gene: HADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.108027713G>A , CM000666.2:g.108027713G>A GRCh38
NC_000004.11:g.108948869G>A , CM000666.1:g.108948869G>A GRCh37
NC_000004.10:g.109168318G>A NCBI36
NG_008156.2:g.42930G>A

Transcript Alleles

HGVS Amino-acid Change
NM_005327.7:c.662G>A MANE Select NP_005318.6:p.Arg221His
ENST00000309522.8:c.662G>A MANE Select ENSP00000312288.4:p.Arg221His
NM_001184705.2:c.662G>A NP_001171634.2:p.Arg221His
NM_001184705.3:c.662G>A NP_001171634.2:p.Arg221His
NM_001184705.4:c.662G>A NP_001171634.3:p.Arg221His
NM_001331027.1:c.674G>A NP_001317956.1:p.Arg225His
NM_001331027.2:c.674G>A NP_001317956.2:p.Arg225His
NM_005327.4:c.662G>A NP_005318.3:p.Arg221His
ENST00000309522.7:c.662G>A ENSP00000312288.3:p.Arg221His
ENST00000403312.5:c.839G>A ENSP00000385638.2:p.Arg280His
ENST00000403312.6:c.662G>A ENSP00000385638.3:p.Arg221His
ENST00000505878.3:c.674G>A ENSP00000425952.1:p.Arg225His
ENST00000505878.4:c.839G>A ENSP00000425952.2:p.Arg280His
ENST00000507260.1:n.362G>A
ENST00000507260.3:n.4872G>A
ENST00000510728.5:n.202G>A
ENST00000510728.6:n.1650G>A
ENST00000514776.2:n.95G>A
ENST00000514776.3:n.95G>A
ENST00000515462.6:n.1849G>A
ENST00000515462.7:n.1849G>A
ENST00000603302.5:c.662G>A ENSP00000474560.1:p.Arg221His
ENST00000626637.1:c.674G>A ENSP00000486771.1:p.Arg225His
ENST00000626637.2:c.674G>A ENSP00000486771.1:p.Arg225His
ENST00000638559.1:c.520G>A
ENST00000638621.1:c.248G>A ENSP00000491581.1:p.Arg83His
ENST00000638648.1:n.813G>A
ENST00000638648.2:c.674G>A ENSP00000507949.1:p.Arg225His
ENST00000639146.1:c.662G>A ENSP00000492345.1:p.Arg221His
ENST00000639335.1:c.*97G>A ENSP00000491310.1:n.*97G>A
ENST00000639698.1:c.516+4150G>A ENSP00000492420.1:n.516+4150G>A
ENST00000639784.1:c.373+4150G>A
ENST00000640048.1:c.634G>A ENSP00000492009.1:n.634G>A
ENST00000640060.1:c.*757G>A ENSP00000492734.1:n.*757G>A
ENST00000640201.1:n.617G>A
ENST00000640201.2:n.748G>A
ENST00000640752.1:n.4865G>A
ENST00000640752.2:n.4872G>A
ENST00000682067.1:c.495G>A
ENST00000682086.1:n.731G>A
ENST00000682373.1:c.321G>A
ENST00000684696.1:c.637-226G>A ENSP00000507675.1:n.637-226G>A
XM_005262972.1:c.674G>A XP_005263029.1:p.Arg225His
XR_001741214.2:n.756G>A
XR_002959727.1:n.756G>A
XR_938726.1:n.811G>A