Canonical Allele Identifier: CA496384005

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974275C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940372C>T , CM000678.2:g.67940372C>T	GRCh38
NC_000016.9:g.67974275C>T , CM000678.1:g.67974275C>T	GRCh37
NC_000016.8:g.66531776C>T	NCBI36
NG_009778.1:g.8741G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.855G>A MANE Select	ENSP00000264005.5:p.Glu285=
ENST00000264005.9:c.855G>A	ENSP00000264005.5:p.Glu285=
ENST00000570369.5:c.156-298G>A
ENST00000570980.1:c.639G>A	ENSP00000464651.1:p.Glu213=
ENST00000573538.5:c.593G>A	ENSP00000463220.1:n.593G>A
NM_000229.1:c.855G>A	NP_000220.1:p.Glu285=
NM_000229.2:c.855G>A MANE Select	NP_000220.1:p.Glu285=