Canonical Allele Identifier: CA2658210801

Gene: HADHA GAREM2

Linked Data

• gnomAD v4: 2-26192394-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26192395del , CM000664.2:g.26192395del	GRCh38
NC_000002.11:g.26415264del , CM000664.1:g.26415264del	GRCh37
NC_000002.10:g.26268768del	NCBI36
NG_007121.1:g.57226del
NG_007121.2:g.57227del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380649.8:c.1915del (HADHA) MANE Select	ENSP00000370023.3:p.Tyr639IlefsTer5
ENST00000492433.2:c.1915del (HADHA)	ENSP00000438039.2:p.Tyr639IlefsTer5
ENST00000643057.1:c.*1806del (HADHA)	ENSP00000493761.1:n.*1806del
ENST00000643063.1:c.*961del (HADHA)	ENSP00000495353.1:n.*961del
ENST00000643233.1:c.*1806del (HADHA)	ENSP00000493880.1:n.*1806del
ENST00000644428.1:c.*539del (HADHA)	ENSP00000495560.1:n.*539del
ENST00000645274.1:c.1810del (HADHA)	ENSP00000493996.1:p.Tyr604IlefsTer5
ENST00000646031.1:c.1274del (HADHA)
ENST00000646483.1:c.1781del (HADHA)	ENSP00000496185.1:n.1781del
ENST00000380649.7:c.1915del (HADHA)	ENSP00000370023.3:p.Tyr639IlefsTer5
ENST00000492433.1:c.373del (HADHA)	ENSP00000438039.1:p.Tyr125IlefsTer5
NM_000182.4:c.1915del (HADHA)	NP_000173.2:p.Tyr639IlefsTer5
XM_011532567.1:c.1683+5080del (GAREM2)	XP_011530869.1:n.1683+5080del
XM_011532567.3:c.1683+5080del (GAREM2)	XP_011530869.1:n.1683+5080del
NM_000182.5:c.1915del (HADHA) MANE Select	NP_000173.2:p.Tyr639IlefsTer5