Canonical Allele Identifier: CA2229564511

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942731T= , CM000678.2:g.67942731T=	GRCh38
NC_000016.9:g.67976634T= , CM000678.1:g.67976634T=	GRCh37
NC_000016.8:g.66534135T=	NCBI36
NG_009778.1:g.6382A=
NG_033098.1:g.30964A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.463A= MANE Select	ENSP00000264005.5:p.Asn155=
ENST00000264005.9:c.463A=	ENSP00000264005.5:p.Asn155=
ENST00000570369.5:c.155+130A=
ENST00000570980.1:c.247A=	ENSP00000464651.1:p.Asn83=
ENST00000573538.5:c.106A=	ENSP00000463220.1:p.Asn36=
ENST00000573846.1:n.77A=
ENST00000575277.1:n.241A=
ENST00000575467.5:c.*158A=	ENSP00000460653.1:n.*158A=
NM_000229.1:c.463A=	NP_000220.1:p.Asn155=
NM_000229.2:c.463A= MANE Select	NP_000220.1:p.Asn155=