Canonical Allele Identifier: CA2633852079

Gene: LCAT

Linked Data

• gnomAD v4: 16-67940832-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940832_67940833insAA , CM000678.2:g.67940832_67940833insAA	GRCh38
NC_000016.9:g.67974735_67974736insAA , CM000678.1:g.67974735_67974736insAA	GRCh37
NC_000016.8:g.66532236_66532237insAA	NCBI36
NG_009778.1:g.8280_8281insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-355_749-354insTT MANE Select	ENSP00000264005.5:n.749-355_749-354insTT
ENST00000264005.9:c.749-355_749-354insTT	ENSP00000264005.5:n.749-355_749-354insTT
ENST00000570369.5:c.156-759_156-758insTT
ENST00000570980.1:c.533-355_533-354insTT	ENSP00000464651.1:n.533-355_533-354insTT
ENST00000573538.5:c.392-2_392-1insTT	ENSP00000463220.1:n.392-2_392-1insTT
NM_000229.1:c.749-355_749-354insTT	NP_000220.1:n.749-355_749-354insTT
NM_000229.2:c.749-355_749-354insTT MANE Select	NP_000220.1:n.749-355_749-354insTT