Canonical Allele Identifier: CA2633851765
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v4: 16-67940760-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940760A>T , CM000678.2:g.67940760A>T GRCh38
NC_000016.9:g.67974663A>T , CM000678.1:g.67974663A>T GRCh37
NC_000016.8:g.66532164A>T NCBI36
NG_009778.1:g.8353T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-282T>A MANE Select ENSP00000264005.5:n.749-282T>A
ENST00000264005.9:c.749-282T>A ENSP00000264005.5:n.749-282T>A
ENST00000570369.5:c.156-686T>A
ENST00000570980.1:c.533-282T>A ENSP00000464651.1:n.533-282T>A
ENST00000573538.5:c.463T>A ENSP00000463220.1:n.463T>A
NM_000229.1:c.749-282T>A NP_000220.1:n.749-282T>A
NM_000229.2:c.749-282T>A MANE Select NP_000220.1:n.749-282T>A
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