Canonical Allele Identifier: CA398706756

Gene: ALDH3A2

Linked Data

• gnomAD v4: 17-19657771-A-T
• MyVariant Identifiers: chr17:g.19561084A>T (hg19) ; chr17:g.19657771A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19657771A>T , CM000679.2:g.19657771A>T	GRCh38
NC_000017.10:g.19561084A>T , CM000679.1:g.19561084A>T	GRCh37
NC_000017.9:g.19501676A>T	NCBI36
NG_007095.2:g.14021A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000176643.11:c.707A>T MANE Select	ENSP00000176643.6:p.Asn236Ile
ENST00000395575.7:c.472-3356A>T	ENSP00000378942.3:n.472-3356A>T
ENST00000472059.6:c.*265A>T	ENSP00000458397.1:n.*265A>T
ENST00000581518.6:c.707A>T	ENSP00000461916.2:p.Asn236Ile
ENST00000582991.6:c.707A>T	ENSP00000464153.1:p.Asn236Ile
ENST00000671841.1:n.2386A>T
ENST00000671878.1:c.707A>T	ENSP00000500516.1:p.Asn236Ile
ENST00000672059.1:n.1158A>T
ENST00000672322.1:n.1778A>T
ENST00000672357.1:c.707A>T	ENSP00000500092.1:p.Asn236Ile
ENST00000672465.1:c.707A>T	ENSP00000500517.1:p.Asn236Ile
ENST00000672487.1:c.680+1197A>T	ENSP00000500740.1:n.680+1197A>T
ENST00000672564.1:n.928A>T
ENST00000672567.1:c.598A>T
ENST00000672608.1:n.1696A>T
ENST00000672709.1:c.561A>T
ENST00000673136.1:c.707A>T	ENSP00000500380.1:p.Asn236Ile
ENST00000673472.1:n.1043A>T
ENST00000176643.10:c.707A>T	ENSP00000176643.6:p.Asn236Ile
ENST00000339618.8:c.707A>T	ENSP00000345774.4:p.Asn236Ile
ENST00000395575.6:c.707A>T	ENSP00000378942.2:p.Asn236Ile
ENST00000472059.5:c.*265A>T	ENSP00000458397.1:n.*265A>T
ENST00000476965.5:n.457A>T
ENST00000571537.1:c.200A>T	ENSP00000458942.1:p.Asn67Ile
ENST00000578696.1:c.138A>T
ENST00000579855.5:c.707A>T	ENSP00000463637.1:p.Asn236Ile
ENST00000581518.5:c.707A>T	ENSP00000461916.1:p.Asn236Ile
ENST00000582991.5:c.707A>T	ENSP00000464153.1:p.Asn236Ile
ENST00000630662.2:c.-275A>T	ENSP00000487353.1:n.-275A>T
ENST00000631291.2:c.707A>T	ENSP00000486085.1:p.Asn236Ile
NM_000382.2:c.707A>T	NP_000373.1:p.Asn236Ile
NM_001031806.1:c.707A>T	NP_001026976.1:p.Asn236Ile
XM_011523732.1:c.707A>T	XP_011522034.1:p.Asn236Ile
XM_011523733.1:c.707A>T	XP_011522035.1:p.Asn236Ile
XM_011523733.2:c.707A>T	XP_011522035.1:p.Asn236Ile
XM_017024355.1:c.707A>T	XP_016879844.1:p.Asn236Ile
XM_017024356.2:c.707A>T	XP_016879845.1:p.Asn236Ile
XM_017024357.1:c.707A>T	XP_016879846.1:p.Asn236Ile
XM_017024358.2:c.707A>T	XP_016879847.1:p.Asn236Ile
XM_024450651.1:c.128A>T	XP_024306419.1:p.Asn43Ile
XM_024450652.1:c.128A>T	XP_024306420.1:p.Asn43Ile
NM_000382.3:c.707A>T MANE Select	NP_000373.1:p.Asn236Ile
NM_001031806.2:c.707A>T	NP_001026976.1:p.Asn236Ile
NM_001369136.1:c.707A>T	NP_001356065.1:p.Asn236Ile
NM_001369137.1:c.707A>T	NP_001356066.1:p.Asn236Ile
NM_001369138.1:c.707A>T	NP_001356067.1:p.Asn236Ile
NM_001369139.1:c.707A>T	NP_001356068.1:p.Asn236Ile
NM_001369146.1:c.707A>T	NP_001356075.1:p.Asn236Ile
NM_001369148.1:c.128A>T	NP_001356077.1:p.Asn43Ile
NM_001369137.2:c.707A>T	NP_001356066.1:p.Asn236Ile
NM_001369138.2:c.707A>T	NP_001356067.1:p.Asn236Ile
NM_001369146.2:c.707A>T	NP_001356075.1:p.Asn236Ile
NM_001369148.2:c.128A>T	NP_001356077.1:p.Asn43Ile