Canonical Allele Identifier: CA2229563354

Gene: LCAT

Genomic Alleles

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

Transcript Alleles

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