Canonical Allele Identifier: CA377706248

Gene: ALDH18A1

Linked Data

• MyVariant Identifiers: chr10:g.97396848A>C (hg19) ; chr10:g.95637091A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95637091A>C , CM000672.2:g.95637091A>C	GRCh38
NC_000010.10:g.97396848A>C , CM000672.1:g.97396848A>C	GRCh37
NC_000010.9:g.97386838A>C	NCBI36
NG_012258.1:g.24720T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371224.7:c.558+2T>G MANE Select	ENSP00000360268.2:n.558+2T>G
ENST00000371221.3:c.558+2T>G	ENSP00000360265.3:n.558+2T>G
ENST00000371224.6:c.558+2T>G	ENSP00000360268.2:n.558+2T>G
NM_001017423.1:c.558+2T>G	NP_001017423.1:n.558+2T>G
NM_002860.3:c.558+2T>G	NP_002851.2:n.558+2T>G
XM_006717933.1:c.558+2T>G	XP_006717996.1:n.558+2T>G
XM_011540001.1:c.225+2T>G	XP_011538303.1:n.225+2T>G
NM_001323412.1:c.225+2T>G	NP_001310341.1:n.225+2T>G
NM_001323413.1:c.558+2T>G	NP_001310342.1:n.558+2T>G
NM_001323414.1:c.558+2T>G	NP_001310343.1:n.558+2T>G
NM_001323415.1:c.558+2T>G	NP_001310344.1:n.558+2T>G
NM_001323416.1:c.225+2T>G	NP_001310345.1:n.225+2T>G
NM_001323417.1:c.453+196T>G	NP_001310346.1:n.453+196T>G
NM_001323418.1:c.225+2T>G	NP_001310347.1:n.225+2T>G
NM_001323419.1:c.-78-3442T>G	NP_001310348.1:n.-78-3442T>G
XM_024448094.1:c.558+2T>G	XP_024303862.1:n.558+2T>G
XM_024448095.1:c.558+2T>G	XP_024303863.1:n.558+2T>G
XM_024448096.1:c.558+2T>G	XP_024303864.1:n.558+2T>G
XM_024448097.1:c.225+2T>G	XP_024303865.1:n.225+2T>G
NM_002860.4:c.558+2T>G MANE Select	NP_002851.2:n.558+2T>G
NM_001017423.2:c.558+2T>G	NP_001017423.1:n.558+2T>G
NM_001323412.2:c.225+2T>G	NP_001310341.1:n.225+2T>G
NM_001323413.2:c.558+2T>G	NP_001310342.1:n.558+2T>G
NM_001323414.2:c.558+2T>G	NP_001310343.1:n.558+2T>G
NM_001323415.2:c.558+2T>G	NP_001310344.1:n.558+2T>G
NM_001323416.2:c.225+2T>G	NP_001310345.1:n.225+2T>G
NM_001323417.2:c.453+196T>G	NP_001310346.1:n.453+196T>G
NM_001323418.2:c.225+2T>G	NP_001310347.1:n.225+2T>G
NM_001323419.2:c.-78-3442T>G	NP_001310348.1:n.-78-3442T>G