Canonical Allele Identifier: CA2229563154

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67939976G= , CM000678.2:g.67939976G=	GRCh38
NC_000016.9:g.67973879G= , CM000678.1:g.67973879G=	GRCh37
NC_000016.8:g.66531380G=	NCBI36
NG_009778.1:g.9137C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.1251C= MANE Select	ENSP00000264005.5:p.Ile417=
ENST00000264005.9:c.1251C=	ENSP00000264005.5:p.Ile417=
ENST00000570369.5:c.254C=
ENST00000573538.5:c.989C=	ENSP00000463220.1:n.989C=
NM_000229.1:c.1251C=	NP_000220.1:p.Ile417=
NM_000229.2:c.1251C= MANE Select	NP_000220.1:p.Ile417=