Canonical Allele Identifier: CA496383921

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974056C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940153C>A , CM000678.2:g.67940153C>A	GRCh38
NC_000016.9:g.67974056C>A , CM000678.1:g.67974056C>A	GRCh37
NC_000016.8:g.66531557C>A	NCBI36
NG_009778.1:g.8960G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1074G>T MANE Select	ENSP00000264005.5:p.Thr358=
ENST00000264005.9:c.1074G>T	ENSP00000264005.5:p.Thr358=
ENST00000570369.5:c.156-79G>T
ENST00000573538.5:c.812G>T	ENSP00000463220.1:n.812G>T
NM_000229.1:c.1074G>T	NP_000220.1:p.Thr358=
NM_000229.2:c.1074G>T MANE Select	NP_000220.1:p.Thr358=