Canonical Allele Identifier: CA496092533

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67973927A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940024A>G , CM000678.2:g.67940024A>G	GRCh38
NC_000016.9:g.67973927A>G , CM000678.1:g.67973927A>G	GRCh37
NC_000016.8:g.66531428A>G	NCBI36
NG_009778.1:g.9089T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1203T>C MANE Select	ENSP00000264005.5:p.His401=
ENST00000264005.9:c.1203T>C	ENSP00000264005.5:p.His401=
ENST00000570369.5:c.206T>C
ENST00000573538.5:c.941T>C	ENSP00000463220.1:n.941T>C
NM_000229.1:c.1203T>C	NP_000220.1:p.His401=
NM_000229.2:c.1203T>C MANE Select	NP_000220.1:p.His401=