Canonical Allele Identifier: CA2229563463
Gene: LCAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940643T= , CM000678.2:g.67940643T= GRCh38
NC_000016.9:g.67974546T= , CM000678.1:g.67974546T= GRCh37
NC_000016.8:g.66532047T= NCBI36
NG_009778.1:g.8470A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-165A= MANE Select ENSP00000264005.5:n.749-165A=
ENST00000264005.9:c.749-165A= ENSP00000264005.5:n.749-165A=
ENST00000570369.5:c.156-569A=
ENST00000570980.1:c.533-165A= ENSP00000464651.1:n.533-165A=
ENST00000573538.5:c.486+94A= ENSP00000463220.1:n.486+94A=
NM_000229.1:c.749-165A= NP_000220.1:n.749-165A=
NM_000229.2:c.749-165A= MANE Select NP_000220.1:n.749-165A=
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