Canonical Allele Identifier: CA2229563152

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939972G= , CM000678.2:g.67939972G=	GRCh38
NC_000016.9:g.67973875G= , CM000678.1:g.67973875G=	GRCh37
NC_000016.8:g.66531376G=	NCBI36
NG_009778.1:g.9141C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1255C= MANE Select	ENSP00000264005.5:p.Leu419=
ENST00000264005.9:c.1255C=	ENSP00000264005.5:p.Leu419=
ENST00000570369.5:c.258C=
ENST00000573538.5:c.993C=	ENSP00000463220.1:n.993C=
NM_000229.1:c.1255C=	NP_000220.1:p.Leu419=
NM_000229.2:c.1255C= MANE Select	NP_000220.1:p.Leu419=