Canonical Allele Identifier: CA2229563308

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940326C= , CM000678.2:g.67940326C=	GRCh38
NC_000016.9:g.67974229C= , CM000678.1:g.67974229C=	GRCh37
NC_000016.8:g.66531730C=	NCBI36
NG_009778.1:g.8787G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.901G= MANE Select	ENSP00000264005.5:p.Asp301=
ENST00000264005.9:c.901G=	ENSP00000264005.5:p.Asp301=
ENST00000570369.5:c.156-252G=
ENST00000570980.1:c.685G=	ENSP00000464651.1:p.Asp229=
ENST00000573538.5:c.639G=	ENSP00000463220.1:n.639G=
NM_000229.1:c.901G=	NP_000220.1:p.Asp301=
NM_000229.2:c.901G= MANE Select	NP_000220.1:p.Asp301=