Canonical Allele Identifier: CA2229563306

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940318T= , CM000678.2:g.67940318T=	GRCh38
NC_000016.9:g.67974221T= , CM000678.1:g.67974221T=	GRCh37
NC_000016.8:g.66531722T=	NCBI36
NG_009778.1:g.8795A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.909A= MANE Select	ENSP00000264005.5:p.Gln303=
ENST00000264005.9:c.909A=	ENSP00000264005.5:p.Gln303=
ENST00000570369.5:c.156-244A=
ENST00000570980.1:c.693A=	ENSP00000464651.1:p.Gln231=
ENST00000573538.5:c.647A=	ENSP00000463220.1:n.647A=
NM_000229.1:c.909A=	NP_000220.1:p.Gln303=
NM_000229.2:c.909A= MANE Select	NP_000220.1:p.Gln303=