Canonical Allele Identifier: CA496384018

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974290G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940387G>T , CM000678.2:g.67940387G>T	GRCh38
NC_000016.9:g.67974290G>T , CM000678.1:g.67974290G>T	GRCh37
NC_000016.8:g.66531791G>T	NCBI36
NG_009778.1:g.8726C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.840C>A MANE Select	ENSP00000264005.5:p.Arg280=
ENST00000264005.9:c.840C>A	ENSP00000264005.5:p.Arg280=
ENST00000570369.5:c.156-313C>A
ENST00000570980.1:c.624C>A	ENSP00000464651.1:p.Arg208=
ENST00000573538.5:c.578C>A	ENSP00000463220.1:n.578C>A
NM_000229.1:c.840C>A	NP_000220.1:p.Arg280=
NM_000229.2:c.840C>A MANE Select	NP_000220.1:p.Arg280=