Canonical Allele Identifier: CA2229564595

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942896T= , CM000678.2:g.67942896T=	GRCh38
NC_000016.9:g.67976799T= , CM000678.1:g.67976799T=	GRCh37
NC_000016.8:g.66534300T=	NCBI36
NG_009778.1:g.6217A=
NG_033098.1:g.30799A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.392A= MANE Select	ENSP00000264005.5:p.Tyr131=
ENST00000264005.9:c.392A=	ENSP00000264005.5:p.Tyr131=
ENST00000570369.5:c.120A=
ENST00000570980.1:c.176A=	ENSP00000464651.1:p.Tyr59=
ENST00000573538.5:c.35A=	ENSP00000463220.1:p.Tyr12=
ENST00000573846.1:n.6A=
ENST00000575277.1:n.170A=
ENST00000575467.5:c.*87A=	ENSP00000460653.1:n.*87A=
NM_000229.1:c.392A=	NP_000220.1:p.Tyr131=
NM_000229.2:c.392A= MANE Select	NP_000220.1:p.Tyr131=