Canonical Allele Identifier: CA2229563164

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940001A= , CM000678.2:g.67940001A=	GRCh38
NC_000016.9:g.67973904A= , CM000678.1:g.67973904A=	GRCh37
NC_000016.8:g.66531405A=	NCBI36
NG_009778.1:g.9112T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1226T= MANE Select	ENSP00000264005.5:p.Leu409=
ENST00000264005.9:c.1226T=	ENSP00000264005.5:p.Leu409=
ENST00000570369.5:c.229T=
ENST00000573538.5:c.964T=	ENSP00000463220.1:n.964T=
NM_000229.1:c.1226T=	NP_000220.1:p.Leu409=
NM_000229.2:c.1226T= MANE Select	NP_000220.1:p.Leu409=