Canonical Allele Identifier: CA396376327
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940427T>A , CM000678.2:g.67940427T>A GRCh38
NC_000016.9:g.67974330T>A , CM000678.1:g.67974330T>A GRCh37
NC_000016.8:g.66531831T>A NCBI36
NG_009778.1:g.8686A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.800A>T MANE Select ENSP00000264005.5:p.Gln267Leu
ENST00000264005.9:c.800A>T ENSP00000264005.5:p.Gln267Leu
ENST00000570369.5:c.156-353A>T
ENST00000570980.1:c.584A>T ENSP00000464651.1:p.Gln195Leu
ENST00000573538.5:c.538A>T ENSP00000463220.1:n.538A>T
NM_000229.1:c.800A>T NP_000220.1:p.Gln267Leu
NM_000229.2:c.800A>T MANE Select NP_000220.1:p.Gln267Leu