Canonical Allele Identifier: CA496092555

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67973933T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940030T>G , CM000678.2:g.67940030T>G	GRCh38
NC_000016.9:g.67973933T>G , CM000678.1:g.67973933T>G	GRCh37
NC_000016.8:g.66531434T>G	NCBI36
NG_009778.1:g.9083A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1197A>C MANE Select	ENSP00000264005.5:p.Ile399=
ENST00000264005.9:c.1197A>C	ENSP00000264005.5:p.Ile399=
ENST00000570369.5:c.200A>C
ENST00000573538.5:c.935A>C	ENSP00000463220.1:n.935A>C
NM_000229.1:c.1197A>C	NP_000220.1:p.Ile399=
NM_000229.2:c.1197A>C MANE Select	NP_000220.1:p.Ile399=