Canonical Allele Identifier: CA2633851380

Gene: LCAT

Linked Data

• gnomAD v4: 16-67940600-T-TGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940600_67940601insGCC , CM000678.2:g.67940600_67940601insGCC	GRCh38
NC_000016.9:g.67974503_67974504insGCC , CM000678.1:g.67974503_67974504insGCC	GRCh37
NC_000016.8:g.66532004_66532005insGCC	NCBI36
NG_009778.1:g.8512_8513insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-123_749-122insGGC MANE Select	ENSP00000264005.5:n.749-123_749-122insGGC
ENST00000264005.9:c.749-123_749-122insGGC	ENSP00000264005.5:n.749-123_749-122insGGC
ENST00000570369.5:c.156-527_156-526insGGC
ENST00000570980.1:c.533-123_533-122insGGC	ENSP00000464651.1:n.533-123_533-122insGGC
ENST00000573538.5:c.487-123_487-122insGGC	ENSP00000463220.1:n.487-123_487-122insGGC
NM_000229.1:c.749-123_749-122insGGC	NP_000220.1:n.749-123_749-122insGGC
NM_000229.2:c.749-123_749-122insGGC MANE Select	NP_000220.1:n.749-123_749-122insGGC