Canonical Allele Identifier: CA2633852039
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940830-CTCTA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940831_67940834del , CM000678.2:g.67940831_67940834del GRCh38
NC_000016.9:g.67974734_67974737del , CM000678.1:g.67974734_67974737del GRCh37
NC_000016.8:g.66532235_66532238del NCBI36
NG_009778.1:g.8279_8282del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-356_749-353del MANE Select ENSP00000264005.5:n.749-356_749-353del
ENST00000264005.9:c.749-356_749-353del ENSP00000264005.5:n.749-356_749-353del
ENST00000570369.5:c.156-760_156-757del
ENST00000570980.1:c.533-356_533-353del ENSP00000464651.1:n.533-356_533-353del
ENST00000573538.5:c.392-3_392del
NM_000229.1:c.749-356_749-353del NP_000220.1:n.749-356_749-353del
NM_000229.2:c.749-356_749-353del MANE Select NP_000220.1:n.749-356_749-353del
Search 100 bp 5'
Search 100 bp 3'