Canonical Allele Identifier: CA2229563552

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940835_67940844delinsCAAAAAAAAA , CM000678.2:g.67940835_67940844delinsCAAAAAAAAA	GRCh38
NC_000016.9:g.67974738_67974747delinsCAAAAAAAAA , CM000678.1:g.67974738_67974747delinsCAAAAAAAAA	GRCh37
NC_000016.8:g.66532239_66532248delinsCAAAAAAAAA	NCBI36
NG_009778.1:g.8269_8278delinsTTTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-366_749-357delinsTTTTTTTTTG MANE Select	ENSP00000264005.5:n.749-366_749-357delinsTTTTTTTTTG
ENST00000264005.9:c.749-366_749-357delinsTTTTTTTTTG	ENSP00000264005.5:n.749-366_749-357delinsTTTTTTTTTG
ENST00000570369.5:c.156-770_156-761delinsTTTTTTTTTG
ENST00000570980.1:c.533-366_533-357delinsTTTTTTTTTG	ENSP00000464651.1:n.533-366_533-357delinsTTTTTTTTTG
ENST00000573538.5:c.392-13_392-4delinsTTTTTTTTTG	ENSP00000463220.1:n.392-13_392-4delinsTTTTTTTTTG
NM_000229.1:c.749-366_749-357delinsTTTTTTTTTG	NP_000220.1:n.749-366_749-357delinsTTTTTTTTTG
NM_000229.2:c.749-366_749-357delinsTTTTTTTTTG MANE Select	NP_000220.1:n.749-366_749-357delinsTTTTTTTTTG