Canonical Allele Identifier: CA1239706468

Gene: HADHA

Linked Data

• dbSNP Id: rs1669922895
• gnomAD v4: 2-26204280-AAACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26204284_26204287del , CM000664.2:g.26204284_26204287del	GRCh38
NC_000002.11:g.26427153_26427156del , CM000664.1:g.26427153_26427156del	GRCh37
NC_000002.10:g.26280657_26280660del	NCBI36
NG_007121.1:g.45337_45340del
NG_007121.2:g.45338_45341del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1086-88_1086-85del MANE Select	ENSP00000370023.3:n.1086-88_1086-85del
ENST00000492433.2:c.1086-88_1086-85del	ENSP00000438039.2:n.1086-88_1086-85del
ENST00000643057.1:c.*977-88_*977-85del	ENSP00000493761.1:n.*977-88_*977-85del
ENST00000643063.1:c.*132-88_*132-85del	ENSP00000495353.1:n.*132-88_*132-85del
ENST00000643233.1:c.*977-88_*977-85del	ENSP00000493880.1:n.*977-88_*977-85del
ENST00000644428.1:c.1086-88_1086-85del	ENSP00000495560.1:n.1086-88_1086-85del
ENST00000645274.1:c.981-88_981-85del	ENSP00000493996.1:n.981-88_981-85del
ENST00000646031.1:c.445-88_445-85del
ENST00000646483.1:c.952-88_952-85del	ENSP00000496185.1:n.952-88_952-85del
ENST00000380649.7:c.1086-88_1086-85del	ENSP00000370023.3:n.1086-88_1086-85del
NM_000182.4:c.1086-88_1086-85del	NP_000173.2:n.1086-88_1086-85del
NM_000182.5:c.1086-88_1086-85del MANE Select	NP_000173.2:n.1086-88_1086-85del