Canonical Allele Identifier: CA2633851385
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940601-A-AATCT
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940602_67940603insTCTA , CM000678.2:g.67940602_67940603insTCTA GRCh38
NC_000016.9:g.67974505_67974506insTCTA , CM000678.1:g.67974505_67974506insTCTA GRCh37
NC_000016.8:g.66532006_66532007insTCTA NCBI36
NG_009778.1:g.8511_8512insAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-124_749-123insAGAT MANE Select ENSP00000264005.5:n.749-124_749-123insAGAT
ENST00000264005.9:c.749-124_749-123insAGAT ENSP00000264005.5:n.749-124_749-123insAGAT
ENST00000570369.5:c.156-528_156-527insAGAT
ENST00000570980.1:c.533-124_533-123insAGAT ENSP00000464651.1:n.533-124_533-123insAGAT
ENST00000573538.5:c.487-124_487-123insAGAT ENSP00000463220.1:n.487-124_487-123insAGAT
NM_000229.1:c.749-124_749-123insAGAT NP_000220.1:n.749-124_749-123insAGAT
NM_000229.2:c.749-124_749-123insAGAT MANE Select NP_000220.1:n.749-124_749-123insAGAT
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