Canonical Allele Identifier: CA496384037

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974317G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940414G>A , CM000678.2:g.67940414G>A	GRCh38
NC_000016.9:g.67974317G>A , CM000678.1:g.67974317G>A	GRCh37
NC_000016.8:g.66531818G>A	NCBI36
NG_009778.1:g.8699C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.813C>T MANE Select	ENSP00000264005.5:p.Thr271=
ENST00000264005.9:c.813C>T	ENSP00000264005.5:p.Thr271=
ENST00000570369.5:c.156-340C>T
ENST00000570980.1:c.597C>T	ENSP00000464651.1:p.Thr199=
ENST00000573538.5:c.551C>T	ENSP00000463220.1:n.551C>T
NM_000229.1:c.813C>T	NP_000220.1:p.Thr271=
NM_000229.2:c.813C>T MANE Select	NP_000220.1:p.Thr271=