Canonical Allele Identifier: CA2576033456
Gene: LCAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940507_67940508insGT , CM000678.2:g.67940507_67940508insGT GRCh38
NC_000016.9:g.67974410_67974411insGT , CM000678.1:g.67974410_67974411insGT GRCh37
NC_000016.8:g.66531911_66531912insGT NCBI36
NG_009778.1:g.8605_8606insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-30_749-29insAC MANE Select ENSP00000264005.5:n.749-30_749-29insAC
ENST00000264005.9:c.749-30_749-29insAC ENSP00000264005.5:n.749-30_749-29insAC
ENST00000570369.5:c.156-434_156-433insAC
ENST00000570980.1:c.533-30_533-29insAC ENSP00000464651.1:n.533-30_533-29insAC
ENST00000573538.5:c.487-30_487-29insAC ENSP00000463220.1:n.487-30_487-29insAC
NM_000229.1:c.749-30_749-29insAC NP_000220.1:n.749-30_749-29insAC
NM_000229.2:c.749-30_749-29insAC MANE Select NP_000220.1:n.749-30_749-29insAC
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