Canonical Allele Identifier: CA2229563295
Gene: LCAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940285G= , CM000678.2:g.67940285G= GRCh38
NC_000016.9:g.67974188G= , CM000678.1:g.67974188G= GRCh37
NC_000016.8:g.66531689G= NCBI36
NG_009778.1:g.8828C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264005.10:c.942C= MANE Select ENSP00000264005.5:p.Gly314=
ENST00000264005.9:c.942C= ENSP00000264005.5:p.Gly314=
ENST00000570369.5:c.156-211C=
ENST00000570980.1:c.726C= ENSP00000464651.1:p.Gly242=
ENST00000573538.5:c.680C= ENSP00000463220.1:n.680C=
NM_000229.1:c.942C= NP_000220.1:p.Gly314=
NM_000229.2:c.942C= MANE Select NP_000220.1:p.Gly314=