Canonical Allele Identifier: CA2229563166

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940007C= , CM000678.2:g.67940007C=	GRCh38
NC_000016.9:g.67973910C= , CM000678.1:g.67973910C=	GRCh37
NC_000016.8:g.66531411C=	NCBI36
NG_009778.1:g.9106G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1220G= MANE Select	ENSP00000264005.5:p.Ser407=
ENST00000264005.9:c.1220G=	ENSP00000264005.5:p.Ser407=
ENST00000570369.5:c.223G=
ENST00000573538.5:c.958G=	ENSP00000463220.1:n.958G=
NM_000229.1:c.1220G=	NP_000220.1:p.Ser407=
NM_000229.2:c.1220G= MANE Select	NP_000220.1:p.Ser407=