Canonical Allele Identifier: CA496092394

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67973888G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939985G>A , CM000678.2:g.67939985G>A	GRCh38
NC_000016.9:g.67973888G>A , CM000678.1:g.67973888G>A	GRCh37
NC_000016.8:g.66531389G>A	NCBI36
NG_009778.1:g.9128C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1242C>T MANE Select	ENSP00000264005.5:p.Ile414=
ENST00000264005.9:c.1242C>T	ENSP00000264005.5:p.Ile414=
ENST00000570369.5:c.245C>T
ENST00000573538.5:c.980C>T	ENSP00000463220.1:n.980C>T
NM_000229.1:c.1242C>T	NP_000220.1:p.Ile414=
NM_000229.2:c.1242C>T MANE Select	NP_000220.1:p.Ile414=