Canonical Allele Identifier: CA496384300

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67976795A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942892A>C , CM000678.2:g.67942892A>C	GRCh38
NC_000016.9:g.67976795A>C , CM000678.1:g.67976795A>C	GRCh37
NC_000016.8:g.66534296A>C	NCBI36
NG_009778.1:g.6221T>G
NG_033098.1:g.30803T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.396T>G MANE Select	ENSP00000264005.5:p.Ser132=
ENST00000264005.9:c.396T>G	ENSP00000264005.5:p.Ser132=
ENST00000570369.5:c.124T>G
ENST00000570980.1:c.180T>G	ENSP00000464651.1:p.Ser60=
ENST00000573538.5:c.39T>G	ENSP00000463220.1:p.Ser13=
ENST00000573846.1:n.10T>G
ENST00000575277.1:n.174T>G
ENST00000575467.5:c.*91T>G	ENSP00000460653.1:n.*91T>G
NM_000229.1:c.396T>G	NP_000220.1:p.Ser132=
NM_000229.2:c.396T>G MANE Select	NP_000220.1:p.Ser132=