Canonical Allele Identifier: CA2229563191
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940067T= , CM000678.2:g.67940067T= GRCh38
NC_000016.9:g.67973970T= , CM000678.1:g.67973970T= GRCh37
NC_000016.8:g.66531471T= NCBI36
NG_009778.1:g.9046A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.1160A= MANE Select ENSP00000264005.5:p.Gln387=
ENST00000264005.9:c.1160A= ENSP00000264005.5:p.Gln387=
ENST00000570369.5:c.163A=
ENST00000573538.5:c.898A= ENSP00000463220.1:n.898A=
NM_000229.1:c.1160A= NP_000220.1:p.Gln387=
NM_000229.2:c.1160A= MANE Select NP_000220.1:p.Gln387=