Canonical Allele Identifier: CA496384126

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974206G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940303G>A , CM000678.2:g.67940303G>A	GRCh38
NC_000016.9:g.67974206G>A , CM000678.1:g.67974206G>A	GRCh37
NC_000016.8:g.66531707G>A	NCBI36
NG_009778.1:g.8810C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.924C>T MANE Select	ENSP00000264005.5:p.Asp308=
ENST00000264005.9:c.924C>T	ENSP00000264005.5:p.Asp308=
ENST00000570369.5:c.156-229C>T
ENST00000570980.1:c.708C>T	ENSP00000464651.1:p.Asp236=
ENST00000573538.5:c.662C>T	ENSP00000463220.1:n.662C>T
NM_000229.1:c.924C>T	NP_000220.1:p.Asp308=
NM_000229.2:c.924C>T MANE Select	NP_000220.1:p.Asp308=