Canonical Allele Identifier: CA3037336

Gene: HADH

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.107990070C>G , CM000666.2:g.107990070C>G	GRCh38
NC_000004.11:g.108911226C>G , CM000666.1:g.108911226C>G	GRCh37
NC_000004.10:g.109130675C>G	NCBI36
NG_008156.2:g.5287C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005327.7:c.132+6C>G MANE Select	NP_005318.6:n.132+6C>G
ENST00000309522.8:c.132+6C>G MANE Select	ENSP00000312288.4:n.132+6C>G
NM_001184705.2:c.132+6C>G	NP_001171634.2:n.132+6C>G
NM_001184705.3:c.132+6C>G	NP_001171634.2:n.132+6C>G
NM_001184705.4:c.132+6C>G	NP_001171634.3:n.132+6C>G
NM_005327.4:c.132+6C>G	NP_005318.3:n.132+6C>G
ENST00000309522.7:c.132+6C>G	ENSP00000312288.3:n.132+6C>G
ENST00000403312.5:c.309+6C>G	ENSP00000385638.2:n.309+6C>G
ENST00000403312.6:c.132+6C>G	ENSP00000385638.3:n.132+6C>G
ENST00000505878.3:c.-111+6C>G	ENSP00000425952.1:n.-111+6C>G
ENST00000505878.4:c.309+6C>G	ENSP00000425952.2:n.309+6C>G
ENST00000507260.2:n.175+6C>G
ENST00000507260.3:n.218+6C>G
ENST00000511742.1:c.132+6C>G	ENSP00000425254.1:n.132+6C>G
ENST00000603302.5:c.132+6C>G	ENSP00000474560.1:n.132+6C>G
ENST00000638559.1:c.119+6C>G
ENST00000638621.1:c.132+6C>G	ENSP00000491581.1:n.132+6C>G
ENST00000639013.1:n.207+6C>G
ENST00000639146.1:c.132+6C>G	ENSP00000492345.1:n.132+6C>G
ENST00000639335.1:c.132+6C>G	ENSP00000491310.1:n.132+6C>G
ENST00000639698.1:c.12+6C>G	ENSP00000492420.1:n.12+6C>G
ENST00000640060.1:c.132+6C>G	ENSP00000492734.1:n.132+6C>G
ENST00000640201.1:n.87+6C>G
ENST00000640201.2:n.218+6C>G
ENST00000640586.1:c.49+6C>G
ENST00000640752.1:n.211+6C>G
ENST00000640752.2:n.218+6C>G
ENST00000681992.1:n.169+6C>G
ENST00000682197.1:n.216+6C>G
ENST00000682373.1:c.76+6C>G
ENST00000684696.1:c.132+6C>G	ENSP00000507675.1:n.132+6C>G
XR_001741214.2:n.226+6C>G
XR_002959727.1:n.226+6C>G
XR_938726.1:n.281+6C>G