Canonical Allele Identifier: CA1929619777

Gene: ALDH18A1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95637179C= , CM000672.2:g.95637179C=	GRCh38
NC_000010.10:g.97396936C= , CM000672.1:g.97396936C=	GRCh37
NC_000010.9:g.97386926C=	NCBI36
NG_012258.1:g.24632G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371224.7:c.472G= MANE Select	ENSP00000360268.2:p.Ala158=
ENST00000371221.3:c.472G=	ENSP00000360265.3:p.Ala158=
ENST00000371224.6:c.472G=	ENSP00000360268.2:p.Ala158=
ENST00000483788.1:n.664G=
NM_001017423.1:c.472G=	NP_001017423.1:p.Ala158=
NM_002860.3:c.472G=	NP_002851.2:p.Ala158=
XM_006717933.1:c.472G=	XP_006717996.1:p.Ala158=
XM_011540001.1:c.139G=	XP_011538303.1:p.Ala47=
NM_001323412.1:c.139G=	NP_001310341.1:p.Ala47=
NM_001323413.1:c.472G=	NP_001310342.1:p.Ala158=
NM_001323414.1:c.472G=	NP_001310343.1:p.Ala158=
NM_001323415.1:c.472G=	NP_001310344.1:p.Ala158=
NM_001323416.1:c.139G=	NP_001310345.1:p.Ala47=
NM_001323417.1:c.453+108G=	NP_001310346.1:n.453+108G=
NM_001323418.1:c.139G=	NP_001310347.1:p.Ala47=
NM_001323419.1:c.-78-3530G=	NP_001310348.1:n.-78-3530G=
XM_024448094.1:c.472G=	XP_024303862.1:p.Ala158=
XM_024448095.1:c.472G=	XP_024303863.1:p.Ala158=
XM_024448096.1:c.472G=	XP_024303864.1:p.Ala158=
XM_024448097.1:c.139G=	XP_024303865.1:p.Ala47=
NM_002860.4:c.472G= MANE Select	NP_002851.2:p.Ala158=
NM_001017423.2:c.472G=	NP_001017423.1:p.Ala158=
NM_001323412.2:c.139G=	NP_001310341.1:p.Ala47=
NM_001323413.2:c.472G=	NP_001310342.1:p.Ala158=
NM_001323414.2:c.472G=	NP_001310343.1:p.Ala158=
NM_001323415.2:c.472G=	NP_001310344.1:p.Ala158=
NM_001323416.2:c.139G=	NP_001310345.1:p.Ala47=
NM_001323417.2:c.453+108G=	NP_001310346.1:n.453+108G=
NM_001323418.2:c.139G=	NP_001310347.1:p.Ala47=
NM_001323419.2:c.-78-3530G=	NP_001310348.1:n.-78-3530G=