Canonical Allele Identifier: CA496383982

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974098G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940195G>C , CM000678.2:g.67940195G>C	GRCh38
NC_000016.9:g.67974098G>C , CM000678.1:g.67974098G>C	GRCh37
NC_000016.8:g.66531599G>C	NCBI36
NG_009778.1:g.8918C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1032C>G MANE Select	ENSP00000264005.5:p.Pro344=
ENST00000264005.9:c.1032C>G	ENSP00000264005.5:p.Pro344=
ENST00000570369.5:c.156-121C>G
ENST00000573538.5:c.770C>G	ENSP00000463220.1:n.770C>G
NM_000229.1:c.1032C>G	NP_000220.1:p.Pro344=
NM_000229.2:c.1032C>G MANE Select	NP_000220.1:p.Pro344=