Canonical Allele Identifier: CA345356310

Gene: LGALS8 HEATR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236540574A>G , CM000663.2:g.236540574A>G	GRCh38
NC_000001.10:g.236703874A>G , CM000663.1:g.236703874A>G	GRCh37
NC_000001.9:g.234770497A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_201544.4:c.356A>G (LGALS8) MANE Select	NP_963838.1:p.Asn119Ser
ENST00000366584.9:c.356A>G (LGALS8) MANE Select	ENSP00000355543.4:p.Asn119Ser
NM_006499.4:c.356A>G (LGALS8)	NP_006490.3:p.Asn119Ser
NM_006499.5:c.356A>G (LGALS8)	NP_006490.3:p.Asn119Ser
NM_201543.2:c.356A>G (LGALS8)	NP_963837.1:p.Asn119Ser
NM_201543.3:c.356A>G (LGALS8)	NP_963837.1:p.Asn119Ser
NM_201543.4:c.356A>G (LGALS8)	NP_963837.1:p.Asn119Ser
NM_201544.2:c.356A>G (LGALS8)	NP_963838.1:p.Asn119Ser
NM_201544.3:c.356A>G (LGALS8)	NP_963838.1:p.Asn119Ser
NM_201545.2:c.356A>G (LGALS8)	NP_963839.1:p.Asn119Ser
ENST00000238181.11:c.345+1485A>G (LGALS8)	ENSP00000238181.7:n.345+1485A>G
ENST00000323938.10:c.275A>G (LGALS8)	ENSP00000434860.1:p.Asn92Ser
ENST00000341872.10:c.356A>G (LGALS8)	ENSP00000342139.6:p.Asn119Ser
ENST00000352231.6:c.356A>G (LGALS8)	ENSP00000309576.2:p.Asn119Ser
ENST00000366583.6:n.532A>G (LGALS8)
ENST00000366584.8:c.356A>G (LGALS8)	ENSP00000355543.4:p.Asn119Ser
ENST00000406509.7:c.356A>G (LGALS8)	ENSP00000385999.3:p.Asn119Ser
ENST00000416919.6:c.345+1485A>G (LGALS8)	ENSP00000410843.2:n.345+1485A>G
ENST00000430527.6:c.346-1080A>G (LGALS8)	ENSP00000398630.2:n.346-1080A>G
ENST00000434231.6:c.*105A>G (LGALS8)	ENSP00000407428.2:n.*105A>G
ENST00000442397.6:c.*176+1485A>G (LGALS8)	ENSP00000413278.2:n.*176+1485A>G
ENST00000450372.6:c.356A>G (LGALS8)	ENSP00000408657.2:p.Asn119Ser
ENST00000454943.6:c.356A>G (LGALS8)	ENSP00000405504.2:p.Asn119Ser
ENST00000525042.1:c.345+1485A>G (LGALS8)	ENSP00000431884.1:n.345+1485A>G
ENST00000526589.5:c.356A>G (LGALS8)	ENSP00000435460.1:p.Asn119Ser
ENST00000526634.5:c.356A>G (LGALS8)	ENSP00000437040.1:p.Asn119Ser
ENST00000527974.5:c.356A>G (LGALS8)	ENSP00000431398.1:p.Asn119Ser
ENST00000528259.5:n.328A>G (LGALS8)
ENST00000528782.5:n.525+1485A>G (LGALS8)
XM_011544188.1:c.356A>G (LGALS8)	XP_011542490.1:p.Asn119Ser
XM_011544188.3:c.356A>G (LGALS8)	XP_011542490.1:p.Asn119Ser
XM_011544219.1:c.*763-3784T>C (HEATR1)	XP_011542521.1:n.*763-3784T>C
XM_017001274.2:c.356A>G (LGALS8)	XP_016856763.1:p.Asn119Ser
XM_017001275.2:c.356A>G (LGALS8)	XP_016856764.1:p.Asn119Ser