Canonical Allele Identifier: CA2633852027
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940829-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940830del , CM000678.2:g.67940830del GRCh38
NC_000016.9:g.67974733del , CM000678.1:g.67974733del GRCh37
NC_000016.8:g.66532234del NCBI36
NG_009778.1:g.8283del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-352del MANE Select ENSP00000264005.5:n.749-352del
ENST00000264005.9:c.749-352del ENSP00000264005.5:n.749-352del
ENST00000570369.5:c.156-756del
ENST00000570980.1:c.533-352del ENSP00000464651.1:n.533-352del
ENST00000573538.5:c.393del ENSP00000463220.1:p.Thr132GlnfsTer?
NM_000229.1:c.749-352del NP_000220.1:n.749-352del
NM_000229.2:c.749-352del MANE Select NP_000220.1:n.749-352del
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