Canonical Allele Identifier: CA2633852071

Gene: LCAT

Linked Data

• gnomAD v4: 16-67940832-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940833_67940834del , CM000678.2:g.67940833_67940834del	GRCh38
NC_000016.9:g.67974736_67974737del , CM000678.1:g.67974736_67974737del	GRCh37
NC_000016.8:g.66532237_66532238del	NCBI36
NG_009778.1:g.8279_8280del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-356_749-355del MANE Select	ENSP00000264005.5:n.749-356_749-355del
ENST00000264005.9:c.749-356_749-355del	ENSP00000264005.5:n.749-356_749-355del
ENST00000570369.5:c.156-760_156-759del
ENST00000570980.1:c.533-356_533-355del	ENSP00000464651.1:n.533-356_533-355del
ENST00000573538.5:c.392-3_392-2del	ENSP00000463220.1:n.392-3_392-2del
NM_000229.1:c.749-356_749-355del	NP_000220.1:n.749-356_749-355del
NM_000229.2:c.749-356_749-355del MANE Select	NP_000220.1:n.749-356_749-355del