Canonical Allele Identifier: CA396376211
Gene: LCAT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67974275C>G (hg19) chr16:g.67940372C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940372C>G , CM000678.2:g.67940372C>G GRCh38
NC_000016.9:g.67974275C>G , CM000678.1:g.67974275C>G GRCh37
NC_000016.8:g.66531776C>G NCBI36
NG_009778.1:g.8741G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.855G>C MANE Select ENSP00000264005.5:p.Glu285Asp
ENST00000264005.9:c.855G>C ENSP00000264005.5:p.Glu285Asp
ENST00000570369.5:c.156-298G>C
ENST00000570980.1:c.639G>C ENSP00000464651.1:p.Glu213Asp
ENST00000573538.5:c.593G>C ENSP00000463220.1:n.593G>C
NM_000229.1:c.855G>C NP_000220.1:p.Glu285Asp
NM_000229.2:c.855G>C MANE Select NP_000220.1:p.Glu285Asp
Search 100 bp 5'
Search 100 bp 3'