Canonical Allele Identifier: CA496383908

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974047C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940144C>G , CM000678.2:g.67940144C>G	GRCh38
NC_000016.9:g.67974047C>G , CM000678.1:g.67974047C>G	GRCh37
NC_000016.8:g.66531548C>G	NCBI36
NG_009778.1:g.8969G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1083G>C MANE Select	ENSP00000264005.5:p.Val361=
ENST00000264005.9:c.1083G>C	ENSP00000264005.5:p.Val361=
ENST00000570369.5:c.156-70G>C
ENST00000573538.5:c.821G>C	ENSP00000463220.1:n.821G>C
NM_000229.1:c.1083G>C	NP_000220.1:p.Val361=
NM_000229.2:c.1083G>C MANE Select	NP_000220.1:p.Val361=