Canonical Allele Identifier: CA2229563480
Gene: LCAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940676C= , CM000678.2:g.67940676C= GRCh38
NC_000016.9:g.67974579C= , CM000678.1:g.67974579C= GRCh37
NC_000016.8:g.66532080C= NCBI36
NG_009778.1:g.8437G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-198G= MANE Select ENSP00000264005.5:n.749-198G=
ENST00000264005.9:c.749-198G= ENSP00000264005.5:n.749-198G=
ENST00000570369.5:c.156-602G=
ENST00000570980.1:c.533-198G= ENSP00000464651.1:n.533-198G=
ENST00000573538.5:c.486+61G= ENSP00000463220.1:n.486+61G=
NM_000229.1:c.749-198G= NP_000220.1:n.749-198G=
NM_000229.2:c.749-198G= MANE Select NP_000220.1:n.749-198G=
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