Canonical Allele Identifier: CA2229563430

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940593_67940595delinsCAG , CM000678.2:g.67940593_67940595delinsCAG	GRCh38
NC_000016.9:g.67974496_67974498delinsCAG , CM000678.1:g.67974496_67974498delinsCAG	GRCh37
NC_000016.8:g.66531997_66531999delinsCAG	NCBI36
NG_009778.1:g.8518_8520delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-117_749-115delinsCTG MANE Select	ENSP00000264005.5:n.749-117_749-115delinsCTG
ENST00000264005.9:c.749-117_749-115delinsCTG	ENSP00000264005.5:n.749-117_749-115delinsCTG
ENST00000570369.5:c.156-521_156-519delinsCTG
ENST00000570980.1:c.533-117_533-115delinsCTG	ENSP00000464651.1:n.533-117_533-115delinsCTG
ENST00000573538.5:c.487-117_487-115delinsCTG	ENSP00000463220.1:n.487-117_487-115delinsCTG
NM_000229.1:c.749-117_749-115delinsCTG	NP_000220.1:n.749-117_749-115delinsCTG
NM_000229.2:c.749-117_749-115delinsCTG MANE Select	NP_000220.1:n.749-117_749-115delinsCTG