Canonical Allele Identifier: CA2636597685

Gene: ALDH3A2

Linked Data

• gnomAD v4: 17-19657705-TTACTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19657706_19657711del , CM000679.2:g.19657706_19657711del	GRCh38
NC_000017.10:g.19561019_19561024del , CM000679.1:g.19561019_19561024del	GRCh37
NC_000017.9:g.19501611_19501616del	NCBI36
NG_007095.2:g.13956_13961del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.681-39_681-34del MANE Select	ENSP00000176643.6:n.681-39_681-34del
ENST00000395575.7:c.472-3421_472-3416del	ENSP00000378942.3:n.472-3421_472-3416del
ENST00000472059.6:c.*239-39_*239-34del	ENSP00000458397.1:n.*239-39_*239-34del
ENST00000581518.6:c.681-39_681-34del	ENSP00000461916.2:n.681-39_681-34del
ENST00000582991.6:c.681-39_681-34del	ENSP00000464153.1:n.681-39_681-34del
ENST00000671841.1:n.2321_2326del
ENST00000671878.1:c.681-39_681-34del	ENSP00000500516.1:n.681-39_681-34del
ENST00000672059.1:n.1132-39_1132-34del
ENST00000672322.1:n.1752-39_1752-34del
ENST00000672357.1:c.681-39_681-34del	ENSP00000500092.1:n.681-39_681-34del
ENST00000672465.1:c.681-39_681-34del	ENSP00000500517.1:n.681-39_681-34del
ENST00000672487.1:c.680+1132_680+1137del	ENSP00000500740.1:n.680+1132_680+1137del
ENST00000672564.1:n.902-39_902-34del
ENST00000672567.1:c.572-39_572-34del
ENST00000672608.1:n.1670-39_1670-34del
ENST00000672709.1:c.535-39_535-34del
ENST00000673136.1:c.681-39_681-34del	ENSP00000500380.1:n.681-39_681-34del
ENST00000673472.1:n.1017-39_1017-34del
ENST00000176643.10:c.681-39_681-34del	ENSP00000176643.6:n.681-39_681-34del
ENST00000339618.8:c.681-39_681-34del	ENSP00000345774.4:n.681-39_681-34del
ENST00000395575.6:c.681-39_681-34del	ENSP00000378942.2:n.681-39_681-34del
ENST00000472059.5:c.*239-39_*239-34del	ENSP00000458397.1:n.*239-39_*239-34del
ENST00000476965.5:n.431-39_431-34del
ENST00000571537.1:c.174-39_174-34del	ENSP00000458942.1:n.174-39_174-34del
ENST00000578696.1:c.88-15_88-10del
ENST00000579855.5:c.681-39_681-34del	ENSP00000463637.1:n.681-39_681-34del
ENST00000581518.5:c.681-39_681-34del	ENSP00000461916.1:n.681-39_681-34del
ENST00000582991.5:c.681-39_681-34del	ENSP00000464153.1:n.681-39_681-34del
ENST00000630662.2:c.-301-39_-301-34del	ENSP00000487353.1:n.-301-39_-301-34del
ENST00000631291.2:c.681-39_681-34del	ENSP00000486085.1:n.681-39_681-34del
NM_000382.2:c.681-39_681-34del	NP_000373.1:n.681-39_681-34del
NM_001031806.1:c.681-39_681-34del	NP_001026976.1:n.681-39_681-34del
XM_011523732.1:c.681-39_681-34del	XP_011522034.1:n.681-39_681-34del
XM_011523733.1:c.681-39_681-34del	XP_011522035.1:n.681-39_681-34del
XM_011523733.2:c.681-39_681-34del	XP_011522035.1:n.681-39_681-34del
XM_017024355.1:c.681-39_681-34del	XP_016879844.1:n.681-39_681-34del
XM_017024356.2:c.681-39_681-34del	XP_016879845.1:n.681-39_681-34del
XM_017024357.1:c.681-39_681-34del	XP_016879846.1:n.681-39_681-34del
XM_017024358.2:c.681-39_681-34del	XP_016879847.1:n.681-39_681-34del
XM_024450651.1:c.102-39_102-34del	XP_024306419.1:n.102-39_102-34del
XM_024450652.1:c.102-39_102-34del	XP_024306420.1:n.102-39_102-34del
NM_000382.3:c.681-39_681-34del MANE Select	NP_000373.1:n.681-39_681-34del
NM_001031806.2:c.681-39_681-34del	NP_001026976.1:n.681-39_681-34del
NM_001369136.1:c.681-39_681-34del	NP_001356065.1:n.681-39_681-34del
NM_001369137.1:c.681-39_681-34del	NP_001356066.1:n.681-39_681-34del
NM_001369138.1:c.681-39_681-34del	NP_001356067.1:n.681-39_681-34del
NM_001369139.1:c.681-39_681-34del	NP_001356068.1:n.681-39_681-34del
NM_001369146.1:c.681-39_681-34del	NP_001356075.1:n.681-39_681-34del
NM_001369148.1:c.102-39_102-34del	NP_001356077.1:n.102-39_102-34del
NM_001369137.2:c.681-39_681-34del	NP_001356066.1:n.681-39_681-34del
NM_001369138.2:c.681-39_681-34del	NP_001356067.1:n.681-39_681-34del
NM_001369146.2:c.681-39_681-34del	NP_001356075.1:n.681-39_681-34del
NM_001369148.2:c.102-39_102-34del	NP_001356077.1:n.102-39_102-34del