Canonical Allele Identifier: CA2633851825
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940779-AC-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940780del , CM000678.2:g.67940780del GRCh38
NC_000016.9:g.67974683del , CM000678.1:g.67974683del GRCh37
NC_000016.8:g.66532184del NCBI36
NG_009778.1:g.8333del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-302del MANE Select ENSP00000264005.5:n.749-302del
ENST00000264005.9:c.749-302del ENSP00000264005.5:n.749-302del
ENST00000570369.5:c.156-706del
ENST00000570980.1:c.533-302del ENSP00000464651.1:n.533-302del
ENST00000573538.5:c.443del ENSP00000463220.1:n.443del
NM_000229.1:c.749-302del NP_000220.1:n.749-302del
NM_000229.2:c.749-302del MANE Select NP_000220.1:n.749-302del
Search 100 bp 5'
Search 100 bp 3'