Canonical Allele Identifier: CA496092461

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67973903C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940000C>A , CM000678.2:g.67940000C>A	GRCh38
NC_000016.9:g.67973903C>A , CM000678.1:g.67973903C>A	GRCh37
NC_000016.8:g.66531404C>A	NCBI36
NG_009778.1:g.9113G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1227G>T MANE Select	ENSP00000264005.5:p.Leu409=
ENST00000264005.9:c.1227G>T	ENSP00000264005.5:p.Leu409=
ENST00000570369.5:c.230G>T
ENST00000573538.5:c.965G>T	ENSP00000463220.1:n.965G>T
NM_000229.1:c.1227G>T	NP_000220.1:p.Leu409=
NM_000229.2:c.1227G>T MANE Select	NP_000220.1:p.Leu409=