Canonical Allele Identifier: CA3037258
Community Standard Title: NC_000004.12:g.107989831G>A
Gene: HADH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.107989831G>A , CM000666.2:g.107989831G>A GRCh38
NC_000004.11:g.108910987G>A , CM000666.1:g.108910987G>A GRCh37
NC_000004.10:g.109130436G>A NCBI36
NG_008156.2:g.5048G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001184705.2:c.-102G>A NP_001171634.2:n.-102G>A
NM_005327.4:c.-102G>A NP_005318.3:n.-102G>A
ENST00000309522.7:c.-102G>A ENSP00000312288.3:n.-102G>A
ENST00000403312.5:c.76G>A ENSP00000385638.2:p.Gly26Ser
ENST00000505878.4:c.76G>A ENSP00000425952.2:p.Gly26Ser
ENST00000603302.5:c.-102G>A ENSP00000474560.1:n.-102G>A
ENST00000639335.1:c.-102G>A ENSP00000491310.1:n.-102G>A
XR_938726.1:n.48G>A