Canonical Allele Identifier: CA5620100

Gene: ALDH18A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95606918C>T , CM000672.2:g.95606918C>T	GRCh38
NC_000010.10:g.97366675C>T , CM000672.1:g.97366675C>T	GRCh37
NC_000010.9:g.97356665C>T	NCBI36
NG_012258.1:g.54893G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371224.7:c.2232G>A MANE Select	ENSP00000360268.2:p.Ser744=
ENST00000371221.3:c.2226G>A	ENSP00000360265.3:p.Ser742=
ENST00000371224.6:c.2232G>A	ENSP00000360268.2:p.Ser744=
NM_001017423.1:c.2226G>A	NP_001017423.1:p.Ser742=
NM_002860.3:c.2232G>A	NP_002851.2:p.Ser744=
XM_006717933.1:c.2232G>A	XP_006717996.1:p.Ser744=
XM_011540001.1:c.1899G>A	XP_011538303.1:p.Ser633=
NM_001323412.1:c.1899G>A	NP_001310341.1:p.Ser633=
NM_001323413.1:c.2232G>A	NP_001310342.1:p.Ser744=
NM_001323414.1:c.2232G>A	NP_001310343.1:p.Ser744=
NM_001323415.1:c.2226G>A	NP_001310344.1:p.Ser742=
NM_001323416.1:c.1899G>A	NP_001310345.1:p.Ser633=
NM_001323417.1:c.2127G>A	NP_001310346.1:p.Ser709=
NM_001323418.1:c.1893G>A	NP_001310347.1:p.Ser631=
NM_001323419.1:c.1596G>A	NP_001310348.1:p.Ser532=
XM_024448094.1:c.2334G>A	XP_024303862.1:p.Ser778=
XM_024448095.1:c.2334G>A	XP_024303863.1:p.Ser778=
XM_024448096.1:c.2328G>A	XP_024303864.1:p.Ser776=
XM_024448097.1:c.2001G>A	XP_024303865.1:p.Ser667=
NM_002860.4:c.2232G>A MANE Select	NP_002851.2:p.Ser744=
NM_001017423.2:c.2226G>A	NP_001017423.1:p.Ser742=
NM_001323412.2:c.1899G>A	NP_001310341.1:p.Ser633=
NM_001323413.2:c.2232G>A	NP_001310342.1:p.Ser744=
NM_001323414.2:c.2232G>A	NP_001310343.1:p.Ser744=
NM_001323415.2:c.2226G>A	NP_001310344.1:p.Ser742=
NM_001323416.2:c.1899G>A	NP_001310345.1:p.Ser633=
NM_001323417.2:c.2127G>A	NP_001310346.1:p.Ser709=
NM_001323418.2:c.1893G>A	NP_001310347.1:p.Ser631=
NM_001323419.2:c.1596G>A	NP_001310348.1:p.Ser532=