Canonical Allele Identifier: CA2229563323

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940358A= , CM000678.2:g.67940358A=	GRCh38
NC_000016.9:g.67974261A= , CM000678.1:g.67974261A=	GRCh37
NC_000016.8:g.66531762A=	NCBI36
NG_009778.1:g.8755T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.869T= MANE Select	ENSP00000264005.5:p.Ile290=
ENST00000264005.9:c.869T=	ENSP00000264005.5:p.Ile290=
ENST00000570369.5:c.156-284T=
ENST00000570980.1:c.653T=	ENSP00000464651.1:p.Ile218=
ENST00000573538.5:c.607T=	ENSP00000463220.1:n.607T=
NM_000229.1:c.869T=	NP_000220.1:p.Ile290=
NM_000229.2:c.869T= MANE Select	NP_000220.1:p.Ile290=