Canonical Allele Identifier: CA396376172
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974258G>T (hg19) chr16:g.67940355G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940355G>T , CM000678.2:g.67940355G>T GRCh38
NC_000016.9:g.67974258G>T , CM000678.1:g.67974258G>T GRCh37
NC_000016.8:g.66531759G>T NCBI36
NG_009778.1:g.8758C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.872C>A MANE Select ENSP00000264005.5:p.Ser291Tyr
ENST00000264005.9:c.872C>A ENSP00000264005.5:p.Ser291Tyr
ENST00000570369.5:c.156-281C>A
ENST00000570980.1:c.656C>A ENSP00000464651.1:p.Ser219Tyr
ENST00000573538.5:c.610C>A ENSP00000463220.1:n.610C>A
NM_000229.1:c.872C>A NP_000220.1:p.Ser291Tyr
NM_000229.2:c.872C>A MANE Select NP_000220.1:p.Ser291Tyr
Search 100 bp 5'
Search 100 bp 3'