Canonical Allele Identifier: CA2229563546

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940832_67940833delinsCT , CM000678.2:g.67940832_67940833delinsCT	GRCh38
NC_000016.9:g.67974735_67974736delinsCT , CM000678.1:g.67974735_67974736delinsCT	GRCh37
NC_000016.8:g.66532236_66532237delinsCT	NCBI36
NG_009778.1:g.8280_8281delinsAG

Transcript Alleles

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