Canonical Allele Identifier: CA496384029

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974308G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940405G>C , CM000678.2:g.67940405G>C	GRCh38
NC_000016.9:g.67974308G>C , CM000678.1:g.67974308G>C	GRCh37
NC_000016.8:g.66531809G>C	NCBI36
NG_009778.1:g.8708C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.822C>G MANE Select	ENSP00000264005.5:p.Pro274=
ENST00000264005.9:c.822C>G	ENSP00000264005.5:p.Pro274=
ENST00000570369.5:c.156-331C>G
ENST00000570980.1:c.606C>G	ENSP00000464651.1:p.Pro202=
ENST00000573538.5:c.560C>G	ENSP00000463220.1:n.560C>G
NM_000229.1:c.822C>G	NP_000220.1:p.Pro274=
NM_000229.2:c.822C>G MANE Select	NP_000220.1:p.Pro274=