Canonical Allele Identifier: CA496384127

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974209T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940306T>A , CM000678.2:g.67940306T>A	GRCh38
NC_000016.9:g.67974209T>A , CM000678.1:g.67974209T>A	GRCh37
NC_000016.8:g.66531710T>A	NCBI36
NG_009778.1:g.8807A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.921A>T MANE Select	ENSP00000264005.5:p.Ala307=
ENST00000264005.9:c.921A>T	ENSP00000264005.5:p.Ala307=
ENST00000570369.5:c.156-232A>T
ENST00000570980.1:c.705A>T	ENSP00000464651.1:p.Ala235=
ENST00000573538.5:c.659A>T	ENSP00000463220.1:n.659A>T
NM_000229.1:c.921A>T	NP_000220.1:p.Ala307=
NM_000229.2:c.921A>T MANE Select	NP_000220.1:p.Ala307=