Canonical Allele Identifier: CA496384202

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67976638G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942735G>C , CM000678.2:g.67942735G>C	GRCh38
NC_000016.9:g.67976638G>C , CM000678.1:g.67976638G>C	GRCh37
NC_000016.8:g.66534139G>C	NCBI36
NG_009778.1:g.6378C>G
NG_033098.1:g.30960C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.459C>G MANE Select	ENSP00000264005.5:p.Val153=
ENST00000264005.9:c.459C>G	ENSP00000264005.5:p.Val153=
ENST00000570369.5:c.155+126C>G
ENST00000570980.1:c.243C>G	ENSP00000464651.1:p.Val81=
ENST00000573538.5:c.102C>G	ENSP00000463220.1:p.Val34=
ENST00000573846.1:n.73C>G
ENST00000575277.1:n.237C>G
ENST00000575467.5:c.*154C>G	ENSP00000460653.1:n.*154C>G
NM_000229.1:c.459C>G	NP_000220.1:p.Val153=
NM_000229.2:c.459C>G MANE Select	NP_000220.1:p.Val153=