Canonical Allele Identifier: CA2229564557

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942803T= , CM000678.2:g.67942803T=	GRCh38
NC_000016.9:g.67976706T= , CM000678.1:g.67976706T=	GRCh37
NC_000016.8:g.66534207T=	NCBI36
NG_009778.1:g.6310A=
NG_033098.1:g.30892A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.428-37A= MANE Select	ENSP00000264005.5:n.428-37A=
ENST00000264005.9:c.428-37A=	ENSP00000264005.5:n.428-37A=
ENST00000570369.5:c.155+58A=
ENST00000570980.1:c.212-37A=	ENSP00000464651.1:n.212-37A=
ENST00000573538.5:c.71-37A=	ENSP00000463220.1:n.71-37A=
ENST00000573846.1:n.42-37A=
ENST00000575277.1:n.206-37A=
ENST00000575467.5:c.*123-37A=	ENSP00000460653.1:n.*123-37A=
NM_000229.1:c.428-37A=	NP_000220.1:n.428-37A=
NM_000229.2:c.428-37A= MANE Select	NP_000220.1:n.428-37A=