Canonical Allele Identifier: CA2229563520

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940753_67940755delinsCTT , CM000678.2:g.67940753_67940755delinsCTT	GRCh38
NC_000016.9:g.67974656_67974658delinsCTT , CM000678.1:g.67974656_67974658delinsCTT	GRCh37
NC_000016.8:g.66532157_66532159delinsCTT	NCBI36
NG_009778.1:g.8358_8360delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-277_749-275delinsAAG MANE Select	ENSP00000264005.5:n.749-277_749-275delinsAAG
ENST00000264005.9:c.749-277_749-275delinsAAG	ENSP00000264005.5:n.749-277_749-275delinsAAG
ENST00000570369.5:c.156-681_156-679delinsAAG
ENST00000570980.1:c.533-277_533-275delinsAAG	ENSP00000464651.1:n.533-277_533-275delinsAAG
ENST00000573538.5:c.468_470delinsAAG	ENSP00000463220.1:n.468_470delinsAAG
NM_000229.1:c.749-277_749-275delinsAAG	NP_000220.1:n.749-277_749-275delinsAAG
NM_000229.2:c.749-277_749-275delinsAAG MANE Select	NP_000220.1:n.749-277_749-275delinsAAG