Canonical Allele Identifier: CA5620496

Gene: ALDH18A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95628482G>A , CM000672.2:g.95628482G>A	GRCh38
NC_000010.10:g.97388239G>A , CM000672.1:g.97388239G>A	GRCh37
NC_000010.9:g.97378229G>A	NCBI36
NG_012258.1:g.33329C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002860.4:c.819C>T MANE Select	NP_002851.2:p.Asp273=
ENST00000371224.7:c.819C>T MANE Select	ENSP00000360268.2:p.Asp273=
NM_001017423.1:c.813C>T	NP_001017423.1:p.Asp271=
NM_001017423.2:c.813C>T	NP_001017423.1:p.Asp271=
NM_001323412.1:c.486C>T	NP_001310341.1:p.Asp162=
NM_001323412.2:c.486C>T	NP_001310341.1:p.Asp162=
NM_001323413.1:c.819C>T	NP_001310342.1:p.Asp273=
NM_001323413.2:c.819C>T	NP_001310342.1:p.Asp273=
NM_001323414.1:c.819C>T	NP_001310343.1:p.Asp273=
NM_001323414.2:c.819C>T	NP_001310343.1:p.Asp273=
NM_001323415.1:c.813C>T	NP_001310344.1:p.Asp271=
NM_001323415.2:c.813C>T	NP_001310344.1:p.Asp271=
NM_001323416.1:c.486C>T	NP_001310345.1:p.Asp162=
NM_001323416.2:c.486C>T	NP_001310345.1:p.Asp162=
NM_001323417.1:c.714C>T	NP_001310346.1:p.Asp238=
NM_001323417.2:c.714C>T	NP_001310346.1:p.Asp238=
NM_001323418.1:c.480C>T	NP_001310347.1:p.Asp160=
NM_001323418.2:c.480C>T	NP_001310347.1:p.Asp160=
NM_001323419.1:c.183C>T	NP_001310348.1:p.Asp61=
NM_001323419.2:c.183C>T	NP_001310348.1:p.Asp61=
NM_002860.3:c.819C>T	NP_002851.2:p.Asp273=
ENST00000371221.3:c.813C>T	ENSP00000360265.3:p.Asp271=
ENST00000371224.6:c.819C>T	ENSP00000360268.2:p.Asp273=
ENST00000489386.1:n.184C>T
XM_006717933.1:c.819C>T	XP_006717996.1:p.Asp273=
XM_011540001.1:c.486C>T	XP_011538303.1:p.Asp162=
XM_024448094.1:c.819C>T	XP_024303862.1:p.Asp273=
XM_024448095.1:c.819C>T	XP_024303863.1:p.Asp273=
XM_024448096.1:c.813C>T	XP_024303864.1:p.Asp271=
XM_024448097.1:c.486C>T	XP_024303865.1:p.Asp162=