Canonical Allele Identifier: CA622937052
Gene: LCAT HGNC NCBI

Linked Data

dbSNP Id: rs1361855303
gnomAD v2: 16-67974735-C-CA
gnomAD v3: 16-67940832-C-CA
gnomAD v4: 16-67940832-C-CA
MyVariant Identifiers: chr16:g.67974735_67974736insA (hg19) chr16:g.67974736delinsAT (hg19) chr16:g.67940832_67940833insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940832_67940833insA , CM000678.2:g.67940832_67940833insA GRCh38
NC_000016.9:g.67974735_67974736insA , CM000678.1:g.67974735_67974736insA GRCh37
NC_000016.8:g.66532236_66532237insA NCBI36
NG_009778.1:g.8280_8281insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-355_749-354insT MANE Select ENSP00000264005.5:n.749-355_749-354insT
ENST00000264005.9:c.749-355_749-354insT ENSP00000264005.5:n.749-355_749-354insT
ENST00000570369.5:c.156-759_156-758insT
ENST00000570980.1:c.533-355_533-354insT ENSP00000464651.1:n.533-355_533-354insT
ENST00000573538.5:c.392-2_392-1insT ENSP00000463220.1:n.392-2_392-1insT
NM_000229.1:c.749-355_749-354insT NP_000220.1:n.749-355_749-354insT
NM_000229.2:c.749-355_749-354insT MANE Select NP_000220.1:n.749-355_749-354insT
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