Canonical Allele Identifier: CA2229563457
Gene: LCAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940635A= , CM000678.2:g.67940635A= GRCh38
NC_000016.9:g.67974538A= , CM000678.1:g.67974538A= GRCh37
NC_000016.8:g.66532039A= NCBI36
NG_009778.1:g.8478T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-157T= MANE Select ENSP00000264005.5:n.749-157T=
ENST00000264005.9:c.749-157T= ENSP00000264005.5:n.749-157T=
ENST00000570369.5:c.156-561T=
ENST00000570980.1:c.533-157T= ENSP00000464651.1:n.533-157T=
ENST00000573538.5:c.486+102T= ENSP00000463220.1:n.486+102T=
NM_000229.1:c.749-157T= NP_000220.1:n.749-157T=
NM_000229.2:c.749-157T= MANE Select NP_000220.1:n.749-157T=
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