Canonical Allele Identifier: CA2229563158

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939988G= , CM000678.2:g.67939988G=	GRCh38
NC_000016.9:g.67973891G= , CM000678.1:g.67973891G=	GRCh37
NC_000016.8:g.66531392G=	NCBI36
NG_009778.1:g.9125C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1239C= MANE Select	ENSP00000264005.5:p.His413=
ENST00000264005.9:c.1239C=	ENSP00000264005.5:p.His413=
ENST00000570369.5:c.242C=
ENST00000573538.5:c.977C=	ENSP00000463220.1:n.977C=
NM_000229.1:c.1239C=	NP_000220.1:p.His413=
NM_000229.2:c.1239C= MANE Select	NP_000220.1:p.His413=