Canonical Allele Identifier: CA5620083
Gene: ALDH18A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 382498
dbSNP Id: rs774047299

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95606805T>G , CM000672.2:g.95606805T>G GRCh38
NC_000010.10:g.97366562T>G , CM000672.1:g.97366562T>G GRCh37
NC_000010.9:g.97356552T>G NCBI36
NG_012258.1:g.55006A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371224.7:c.2345A>C MANE Select ENSP00000360268.2:p.Tyr782Ser
ENST00000371221.3:c.2339A>C ENSP00000360265.3:p.Tyr780Ser
ENST00000371224.6:c.2345A>C ENSP00000360268.2:p.Tyr782Ser
NM_001017423.1:c.2339A>C NP_001017423.1:p.Tyr780Ser
NM_002860.3:c.2345A>C NP_002851.2:p.Tyr782Ser
XM_006717933.1:c.2345A>C XP_006717996.1:p.Tyr782Ser
XM_011540001.1:c.2012A>C XP_011538303.1:p.Tyr671Ser
NM_001323412.1:c.2012A>C NP_001310341.1:p.Tyr671Ser
NM_001323413.1:c.2345A>C NP_001310342.1:p.Tyr782Ser
NM_001323414.1:c.2345A>C NP_001310343.1:p.Tyr782Ser
NM_001323415.1:c.2339A>C NP_001310344.1:p.Tyr780Ser
NM_001323416.1:c.2012A>C NP_001310345.1:p.Tyr671Ser
NM_001323417.1:c.2240A>C NP_001310346.1:p.Tyr747Ser
NM_001323418.1:c.2006A>C NP_001310347.1:p.Tyr669Ser
NM_001323419.1:c.1709A>C NP_001310348.1:p.Tyr570Ser
XM_024448094.1:c.2447A>C XP_024303862.1:p.Tyr816Ser
XM_024448095.1:c.2447A>C XP_024303863.1:p.Tyr816Ser
XM_024448096.1:c.2441A>C XP_024303864.1:p.Tyr814Ser
XM_024448097.1:c.2114A>C XP_024303865.1:p.Tyr705Ser
NM_002860.4:c.2345A>C MANE Select NP_002851.2:p.Tyr782Ser
NM_001017423.2:c.2339A>C NP_001017423.1:p.Tyr780Ser
NM_001323412.2:c.2012A>C NP_001310341.1:p.Tyr671Ser
NM_001323413.2:c.2345A>C NP_001310342.1:p.Tyr782Ser
NM_001323414.2:c.2345A>C NP_001310343.1:p.Tyr782Ser
NM_001323415.2:c.2339A>C NP_001310344.1:p.Tyr780Ser
NM_001323416.2:c.2012A>C NP_001310345.1:p.Tyr671Ser
NM_001323417.2:c.2240A>C NP_001310346.1:p.Tyr747Ser
NM_001323418.2:c.2006A>C NP_001310347.1:p.Tyr669Ser
NM_001323419.2:c.1709A>C NP_001310348.1:p.Tyr570Ser