Canonical Allele Identifier: CA2229563322

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940357A= , CM000678.2:g.67940357A=	GRCh38
NC_000016.9:g.67974260A= , CM000678.1:g.67974260A=	GRCh37
NC_000016.8:g.66531761A=	NCBI36
NG_009778.1:g.8756T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.870T= MANE Select	ENSP00000264005.5:p.Ile290=
ENST00000264005.9:c.870T=	ENSP00000264005.5:p.Ile290=
ENST00000570369.5:c.156-283T=
ENST00000570980.1:c.654T=	ENSP00000464651.1:p.Ile218=
ENST00000573538.5:c.608T=	ENSP00000463220.1:n.608T=
NM_000229.1:c.870T=	NP_000220.1:p.Ile290=
NM_000229.2:c.870T= MANE Select	NP_000220.1:p.Ile290=