Canonical Allele Identifier: CA396376242
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940385A>C , CM000678.2:g.67940385A>C GRCh38
NC_000016.9:g.67974288A>C , CM000678.1:g.67974288A>C GRCh37
NC_000016.8:g.66531789A>C NCBI36
NG_009778.1:g.8728T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264005.10:c.842T>G MANE Select ENSP00000264005.5:p.Met281Arg
ENST00000264005.9:c.842T>G ENSP00000264005.5:p.Met281Arg
ENST00000570369.5:c.156-311T>G
ENST00000570980.1:c.626T>G ENSP00000464651.1:p.Met209Arg
ENST00000573538.5:c.580T>G ENSP00000463220.1:n.580T>G
NM_000229.1:c.842T>G NP_000220.1:p.Met281Arg
NM_000229.2:c.842T>G MANE Select NP_000220.1:p.Met281Arg