Canonical Allele Identifier: CA2636595938

Gene: ALDH3A2

Linked Data

• gnomAD v4: 17-19648809-TGAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19648818_19648821del , CM000679.2:g.19648818_19648821del	GRCh38
NC_000017.10:g.19552131_19552134del , CM000679.1:g.19552131_19552134del	GRCh37
NC_000017.9:g.19492723_19492726del	NCBI36
NG_007095.2:g.5068_5071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176643.11:c.-154_-151del MANE Select	ENSP00000176643.6:n.-154_-151del
ENST00000395575.7:c.-154_-151del	ENSP00000378942.3:n.-154_-151del
ENST00000467473.6:n.87-117_87-114del
ENST00000581518.6:c.-37-117_-37-114del	ENSP00000461916.2:n.-37-117_-37-114del
ENST00000582991.6:c.-63_-60del	ENSP00000464153.1:n.-63_-60del
ENST00000671878.1:c.-154_-151del	ENSP00000500516.1:n.-154_-151del
ENST00000672357.1:c.-63_-60del	ENSP00000500092.1:n.-63_-60del
ENST00000672465.1:c.-37-117_-37-114del	ENSP00000500517.1:n.-37-117_-37-114del
ENST00000672487.1:c.-154_-151del	ENSP00000500740.1:n.-154_-151del
ENST00000672564.1:n.68_71del
ENST00000673136.1:c.-37-117_-37-114del	ENSP00000500380.1:n.-37-117_-37-114del
ENST00000176643.10:c.-154_-151del	ENSP00000176643.6:n.-154_-151del
ENST00000339618.8:c.-154_-151del	ENSP00000345774.4:n.-154_-151del
ENST00000395575.6:c.-63_-60del	ENSP00000378942.2:n.-63_-60del
ENST00000446398.6:c.-37-117_-37-114del	ENSP00000395845.2:n.-37-117_-37-114del
ENST00000467473.5:n.121-117_121-114del
ENST00000578614.1:c.-154_-151del	ENSP00000463128.1:n.-154_-151del
ENST00000579855.5:c.-32_-29del	ENSP00000463637.1:n.-32_-29del
ENST00000580550.5:c.-9-145_-9-142del	ENSP00000462964.1:n.-9-145_-9-142del
ENST00000581518.5:c.-154_-151del	ENSP00000461916.1:n.-154_-151del
ENST00000582991.5:c.-154_-151del	ENSP00000464153.1:n.-154_-151del
ENST00000584332.6:c.-126_-123del	ENSP00000466814.1:n.-126_-123del
ENST00000626500.2:c.-154_-151del	ENSP00000486283.1:n.-154_-151del
ENST00000630662.2:c.-1135_-1132del	ENSP00000487353.1:n.-1135_-1132del
ENST00000631291.2:c.-154_-151del	ENSP00000486085.1:n.-154_-151del
NM_000382.2:c.-154_-151del	NP_000373.1:n.-154_-151del
NM_001031806.1:c.-154_-151del	NP_001026976.1:n.-154_-151del
XM_011523732.1:c.-63_-60del	XP_011522034.1:n.-63_-60del
XM_011523733.1:c.-37-117_-37-114del	XP_011522035.1:n.-37-117_-37-114del
XM_011523733.2:c.-37-117_-37-114del	XP_011522035.1:n.-37-117_-37-114del
XM_017024356.2:c.-37-117_-37-114del	XP_016879845.1:n.-37-117_-37-114del
XM_017024357.1:c.-63_-60del	XP_016879846.1:n.-63_-60del
XM_017024358.2:c.-37-117_-37-114del	XP_016879847.1:n.-37-117_-37-114del
XM_024450652.1:c.-725-117_-725-114del	XP_024306420.1:n.-725-117_-725-114del
NM_000382.3:c.-154_-151del MANE Select	NP_000373.1:n.-154_-151del
NM_001031806.2:c.-154_-151del	NP_001026976.1:n.-154_-151del
NM_001369136.1:c.-63_-60del	NP_001356065.1:n.-63_-60del
NM_001369137.1:c.-37-117_-37-114del	NP_001356066.1:n.-37-117_-37-114del
NM_001369138.1:c.-37-117_-37-114del	NP_001356067.1:n.-37-117_-37-114del
NM_001369139.1:c.-63_-60del	NP_001356068.1:n.-63_-60del
NM_001369146.1:c.-37-117_-37-114del	NP_001356075.1:n.-37-117_-37-114del
NM_001369148.1:c.-725-117_-725-114del	NP_001356077.1:n.-725-117_-725-114del
NM_001369137.2:c.-37-117_-37-114del	NP_001356066.1:n.-37-117_-37-114del
NM_001369138.2:c.-37-117_-37-114del	NP_001356067.1:n.-37-117_-37-114del
NM_001369146.2:c.-37-117_-37-114del	NP_001356075.1:n.-37-117_-37-114del
NM_001369148.2:c.-725-117_-725-114del	NP_001356077.1:n.-725-117_-725-114del