Canonical Allele Identifier: CA2229563525

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940763C= , CM000678.2:g.67940763C=	GRCh38
NC_000016.9:g.67974666C= , CM000678.1:g.67974666C=	GRCh37
NC_000016.8:g.66532167C=	NCBI36
NG_009778.1:g.8350G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-285G= MANE Select	ENSP00000264005.5:n.749-285G=
ENST00000264005.9:c.749-285G=	ENSP00000264005.5:n.749-285G=
ENST00000570369.5:c.156-689G=
ENST00000570980.1:c.533-285G=	ENSP00000464651.1:n.533-285G=
ENST00000573538.5:c.460G=	ENSP00000463220.1:n.460G=
NM_000229.1:c.749-285G=	NP_000220.1:n.749-285G=
NM_000229.2:c.749-285G= MANE Select	NP_000220.1:n.749-285G=