Canonical Allele Identifier: CA396376034
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974197A>T (hg19) chr16:g.67940294A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940294A>T , CM000678.2:g.67940294A>T GRCh38
NC_000016.9:g.67974197A>T , CM000678.1:g.67974197A>T GRCh37
NC_000016.8:g.66531698A>T NCBI36
NG_009778.1:g.8819T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.933T>A MANE Select ENSP00000264005.5:p.Phe311Leu
ENST00000264005.9:c.933T>A ENSP00000264005.5:p.Phe311Leu
ENST00000570369.5:c.156-220T>A
ENST00000570980.1:c.717T>A ENSP00000464651.1:p.Phe239Leu
ENST00000573538.5:c.671T>A ENSP00000463220.1:n.671T>A
NM_000229.1:c.933T>A NP_000220.1:p.Phe311Leu
NM_000229.2:c.933T>A MANE Select NP_000220.1:p.Phe311Leu
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