Canonical Allele Identifier: CA1929619752
Gene: ALDH18A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95637088C= , CM000672.2:g.95637088C= GRCh38
NC_000010.10:g.97396845C= , CM000672.1:g.97396845C= GRCh37
NC_000010.9:g.97386835C= NCBI36
NG_012258.1:g.24723G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371224.7:c.558+5G= MANE Select ENSP00000360268.2:n.558+5G=
ENST00000371221.3:c.558+5G= ENSP00000360265.3:n.558+5G=
ENST00000371224.6:c.558+5G= ENSP00000360268.2:n.558+5G=
NM_001017423.1:c.558+5G= NP_001017423.1:n.558+5G=
NM_002860.3:c.558+5G= NP_002851.2:n.558+5G=
XM_006717933.1:c.558+5G= XP_006717996.1:n.558+5G=
XM_011540001.1:c.225+5G= XP_011538303.1:n.225+5G=
NM_001323412.1:c.225+5G= NP_001310341.1:n.225+5G=
NM_001323413.1:c.558+5G= NP_001310342.1:n.558+5G=
NM_001323414.1:c.558+5G= NP_001310343.1:n.558+5G=
NM_001323415.1:c.558+5G= NP_001310344.1:n.558+5G=
NM_001323416.1:c.225+5G= NP_001310345.1:n.225+5G=
NM_001323417.1:c.453+199G= NP_001310346.1:n.453+199G=
NM_001323418.1:c.225+5G= NP_001310347.1:n.225+5G=
NM_001323419.1:c.-78-3439G= NP_001310348.1:n.-78-3439G=
XM_024448094.1:c.558+5G= XP_024303862.1:n.558+5G=
XM_024448095.1:c.558+5G= XP_024303863.1:n.558+5G=
XM_024448096.1:c.558+5G= XP_024303864.1:n.558+5G=
XM_024448097.1:c.225+5G= XP_024303865.1:n.225+5G=
NM_002860.4:c.558+5G= MANE Select NP_002851.2:n.558+5G=
NM_001017423.2:c.558+5G= NP_001017423.1:n.558+5G=
NM_001323412.2:c.225+5G= NP_001310341.1:n.225+5G=
NM_001323413.2:c.558+5G= NP_001310342.1:n.558+5G=
NM_001323414.2:c.558+5G= NP_001310343.1:n.558+5G=
NM_001323415.2:c.558+5G= NP_001310344.1:n.558+5G=
NM_001323416.2:c.225+5G= NP_001310345.1:n.225+5G=
NM_001323417.2:c.453+199G= NP_001310346.1:n.453+199G=
NM_001323418.2:c.225+5G= NP_001310347.1:n.225+5G=
NM_001323419.2:c.-78-3439G= NP_001310348.1:n.-78-3439G=