Canonical Allele Identifier: CA2633852034
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940830-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940831del , CM000678.2:g.67940831del GRCh38
NC_000016.9:g.67974734del , CM000678.1:g.67974734del GRCh37
NC_000016.8:g.66532235del NCBI36
NG_009778.1:g.8282del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-353del MANE Select ENSP00000264005.5:n.749-353del
ENST00000264005.9:c.749-353del ENSP00000264005.5:n.749-353del
ENST00000570369.5:c.156-757del
ENST00000570980.1:c.533-353del ENSP00000464651.1:n.533-353del
ENST00000573538.5:c.392del ENSP00000463220.1:p.Glu131GlyfsTer?
NM_000229.1:c.749-353del NP_000220.1:n.749-353del
NM_000229.2:c.749-353del MANE Select NP_000220.1:n.749-353del
Search 100 bp 5'
Search 100 bp 3'