Canonical Allele Identifier: CA496384052

Gene: LCAT

Linked Data

• MyVariant Identifiers: chr16:g.67974341C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940438C>A , CM000678.2:g.67940438C>A	GRCh38
NC_000016.9:g.67974341C>A , CM000678.1:g.67974341C>A	GRCh37
NC_000016.8:g.66531842C>A	NCBI36
NG_009778.1:g.8675G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.789G>T MANE Select	ENSP00000264005.5:p.Leu263=
ENST00000264005.9:c.789G>T	ENSP00000264005.5:p.Leu263=
ENST00000570369.5:c.156-364G>T
ENST00000570980.1:c.573G>T	ENSP00000464651.1:p.Leu191=
ENST00000573538.5:c.527G>T	ENSP00000463220.1:n.527G>T
NM_000229.1:c.789G>T	NP_000220.1:p.Leu263=
NM_000229.2:c.789G>T MANE Select	NP_000220.1:p.Leu263=