Canonical Allele Identifier: CA2633851743
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940750-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940751del , CM000678.2:g.67940751del GRCh38
NC_000016.9:g.67974654del , CM000678.1:g.67974654del GRCh37
NC_000016.8:g.66532155del NCBI36
NG_009778.1:g.8362del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-273del MANE Select ENSP00000264005.5:n.749-273del
ENST00000264005.9:c.749-273del ENSP00000264005.5:n.749-273del
ENST00000570369.5:c.156-677del
ENST00000570980.1:c.533-273del ENSP00000464651.1:n.533-273del
ENST00000573538.5:c.472del ENSP00000463220.1:n.472del
NM_000229.1:c.749-273del NP_000220.1:n.749-273del
NM_000229.2:c.749-273del MANE Select NP_000220.1:n.749-273del
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Search 100 bp 3'