Canonical Allele Identifier: CA2229563452
Gene: LCAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940626T= , CM000678.2:g.67940626T= GRCh38
NC_000016.9:g.67974529T= , CM000678.1:g.67974529T= GRCh37
NC_000016.8:g.66532030T= NCBI36
NG_009778.1:g.8487A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-148A= MANE Select ENSP00000264005.5:n.749-148A=
ENST00000264005.9:c.749-148A= ENSP00000264005.5:n.749-148A=
ENST00000570369.5:c.156-552A=
ENST00000570980.1:c.533-148A= ENSP00000464651.1:n.533-148A=
ENST00000573538.5:c.486+111A= ENSP00000463220.1:n.486+111A=
NM_000229.1:c.749-148A= NP_000220.1:n.749-148A=
NM_000229.2:c.749-148A= MANE Select NP_000220.1:n.749-148A=
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