Canonical Allele Identifier: CA2229564609

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942927G= , CM000678.2:g.67942927G=	GRCh38
NC_000016.9:g.67976830G= , CM000678.1:g.67976830G=	GRCh37
NC_000016.8:g.66534331G=	NCBI36
NG_009778.1:g.6186C=
NG_033098.1:g.30768C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.361C= MANE Select	ENSP00000264005.5:p.Gln121=
ENST00000264005.9:c.361C=	ENSP00000264005.5:p.Gln121=
ENST00000570369.5:c.89C=
ENST00000570980.1:c.145C=	ENSP00000464651.1:p.Gln49=
ENST00000573538.5:c.4C=	ENSP00000463220.1:p.Gln2=
ENST00000575277.1:n.139C=
ENST00000575467.5:c.*56C=	ENSP00000460653.1:n.*56C=
NM_000229.1:c.361C=	NP_000220.1:p.Gln121=
NM_000229.2:c.361C= MANE Select	NP_000220.1:p.Gln121=