Canonical Allele Identifier: CA5620258
Community Standard Title: NM_002860.4(ALDH18A1):c.1624G>A (p.Val542Ile)
Gene: ALDH18A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95614143C>T , CM000672.2:g.95614143C>T GRCh38
NC_000010.10:g.97373900C>T , CM000672.1:g.97373900C>T GRCh37
NC_000010.9:g.97363890C>T NCBI36
NG_012258.1:g.47668G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002860.4:c.1624G>A MANE Select NP_002851.2:p.Val542Ile
ENST00000371224.7:c.1624G>A MANE Select ENSP00000360268.2:p.Val542Ile
NM_001017423.1:c.1618G>A NP_001017423.1:p.Val540Ile
NM_001017423.2:c.1618G>A NP_001017423.1:p.Val540Ile
NM_001323412.1:c.1291G>A NP_001310341.1:p.Val431Ile
NM_001323412.2:c.1291G>A NP_001310341.1:p.Val431Ile
NM_001323413.1:c.1624G>A NP_001310342.1:p.Val542Ile
NM_001323413.2:c.1624G>A NP_001310342.1:p.Val542Ile
NM_001323414.1:c.1624G>A NP_001310343.1:p.Val542Ile
NM_001323414.2:c.1624G>A NP_001310343.1:p.Val542Ile
NM_001323415.1:c.1618G>A NP_001310344.1:p.Val540Ile
NM_001323415.2:c.1618G>A NP_001310344.1:p.Val540Ile
NM_001323416.1:c.1291G>A NP_001310345.1:p.Val431Ile
NM_001323416.2:c.1291G>A NP_001310345.1:p.Val431Ile
NM_001323417.1:c.1519G>A NP_001310346.1:p.Val507Ile
NM_001323417.2:c.1519G>A NP_001310346.1:p.Val507Ile
NM_001323418.1:c.1285G>A NP_001310347.1:p.Val429Ile
NM_001323418.2:c.1285G>A NP_001310347.1:p.Val429Ile
NM_001323419.1:c.988G>A NP_001310348.1:p.Val330Ile
NM_001323419.2:c.988G>A NP_001310348.1:p.Val330Ile
NM_002860.3:c.1624G>A NP_002851.2:p.Val542Ile
ENST00000371221.3:c.1618G>A ENSP00000360265.3:p.Val540Ile
ENST00000371224.6:c.1624G>A ENSP00000360268.2:p.Val542Ile
ENST00000485428.1:n.240G>A
XM_006717933.1:c.1624G>A XP_006717996.1:p.Val542Ile
XM_011540001.1:c.1291G>A XP_011538303.1:p.Val431Ile
XM_024448094.1:c.1624G>A XP_024303862.1:p.Val542Ile
XM_024448095.1:c.1624G>A XP_024303863.1:p.Val542Ile
XM_024448096.1:c.1618G>A XP_024303864.1:p.Val540Ile
XM_024448097.1:c.1291G>A XP_024303865.1:p.Val431Ile