Canonical Allele Identifier: CA2229563387

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940513G= , CM000678.2:g.67940513G=	GRCh38
NC_000016.9:g.67974416G= , CM000678.1:g.67974416G=	GRCh37
NC_000016.8:g.66531917G=	NCBI36
NG_009778.1:g.8600C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.749-35C= MANE Select	ENSP00000264005.5:n.749-35C=
ENST00000264005.9:c.749-35C=	ENSP00000264005.5:n.749-35C=
ENST00000570369.5:c.156-439C=
ENST00000570980.1:c.533-35C=	ENSP00000464651.1:n.533-35C=
ENST00000573538.5:c.487-35C=	ENSP00000463220.1:n.487-35C=
NM_000229.1:c.749-35C=	NP_000220.1:n.749-35C=
NM_000229.2:c.749-35C= MANE Select	NP_000220.1:n.749-35C=