Canonical Allele Identifier: CA2229564615

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942937G= , CM000678.2:g.67942937G=	GRCh38
NC_000016.9:g.67976840G= , CM000678.1:g.67976840G=	GRCh37
NC_000016.8:g.66534341G=	NCBI36
NG_009778.1:g.6176C=
NG_033098.1:g.30758C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.351C= MANE Select	ENSP00000264005.5:p.Ala117=
ENST00000264005.9:c.351C=	ENSP00000264005.5:p.Ala117=
ENST00000570369.5:c.79C=
ENST00000570980.1:c.135C=	ENSP00000464651.1:p.Ala45=
ENST00000575277.1:n.129C=
ENST00000575467.5:c.*46C=	ENSP00000460653.1:n.*46C=
NM_000229.1:c.351C=	NP_000220.1:p.Ala117=
NM_000229.2:c.351C= MANE Select	NP_000220.1:p.Ala117=