Canonical Allele Identifier: CA2229563222

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940129C= , CM000678.2:g.67940129C=	GRCh38
NC_000016.9:g.67974032C= , CM000678.1:g.67974032C=	GRCh37
NC_000016.8:g.66531533C=	NCBI36
NG_009778.1:g.8984G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1098G= MANE Select	ENSP00000264005.5:p.Glu366=
ENST00000264005.9:c.1098G=	ENSP00000264005.5:p.Glu366=
ENST00000570369.5:c.156-55G=
ENST00000573538.5:c.836G=	ENSP00000463220.1:n.836G=
NM_000229.1:c.1098G=	NP_000220.1:p.Glu366=
NM_000229.2:c.1098G= MANE Select	NP_000220.1:p.Glu366=