Canonical Allele Identifier: CA931581928

Gene: HOGA1

Linked Data

• dbSNP Id: rs2041103150
• gnomAD v3: 10-97599927-TTCTC-T
• gnomAD v4: 10-97599927-TTCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.97599931_97599934del , CM000672.2:g.97599931_97599934del	GRCh38
NC_000010.10:g.99359688_99359691del , CM000672.1:g.99359688_99359691del	GRCh37
NC_000010.9:g.99349678_99349681del	NCBI36
NG_027922.1:g.20587_20590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370646.9:c.603+117_603+120del MANE Select	ENSP00000359680.4:n.603+117_603+120del
ENST00000370642.4:c.13+117_13+120del
ENST00000370646.8:c.603+117_603+120del	ENSP00000359680.4:n.603+117_603+120del
ENST00000370647.8:c.212-1926_212-1923del	ENSP00000359681.4:n.212-1926_212-1923del
ENST00000370649.3:c.212-1926_212-1923del	ENSP00000359683.3:n.212-1926_212-1923del
ENST00000465608.1:n.1564_1567del
NM_001134670.1:c.212-1926_212-1923del	NP_001128142.1:n.212-1926_212-1923del
NM_138413.3:c.603+117_603+120del	NP_612422.2:n.603+117_603+120del
NM_138413.4:c.603+117_603+120del MANE Select	NP_612422.2:n.603+117_603+120del
NM_001134670.2:c.212-1926_212-1923del	NP_001128142.1:n.212-1926_212-1923del