Canonical Allele Identifier: CA2633852135

Gene: LCAT

Linked Data

• gnomAD v4: 16-67940834-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940834_67940835insG , CM000678.2:g.67940834_67940835insG	GRCh38
NC_000016.9:g.67974737_67974738insG , CM000678.1:g.67974737_67974738insG	GRCh37
NC_000016.8:g.66532238_66532239insG	NCBI36
NG_009778.1:g.8278_8279insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-357_749-356insC MANE Select	ENSP00000264005.5:n.749-357_749-356insC
ENST00000264005.9:c.749-357_749-356insC	ENSP00000264005.5:n.749-357_749-356insC
ENST00000570369.5:c.156-761_156-760insC
ENST00000570980.1:c.533-357_533-356insC	ENSP00000464651.1:n.533-357_533-356insC
ENST00000573538.5:c.392-4_392-3insC	ENSP00000463220.1:n.392-4_392-3insC
NM_000229.1:c.749-357_749-356insC	NP_000220.1:n.749-357_749-356insC
NM_000229.2:c.749-357_749-356insC MANE Select	NP_000220.1:n.749-357_749-356insC