Canonical Allele Identifier: CA2229563357

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940441C= , CM000678.2:g.67940441C=	GRCh38
NC_000016.9:g.67974344C= , CM000678.1:g.67974344C=	GRCh37
NC_000016.8:g.66531845C=	NCBI36
NG_009778.1:g.8672G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.786G= MANE Select	ENSP00000264005.5:p.Lys262=
ENST00000264005.9:c.786G=	ENSP00000264005.5:p.Lys262=
ENST00000570369.5:c.156-367G=
ENST00000570980.1:c.570G=	ENSP00000464651.1:p.Lys190=
ENST00000573538.5:c.524G=	ENSP00000463220.1:n.524G=
NM_000229.1:c.786G=	NP_000220.1:p.Lys262=
NM_000229.2:c.786G= MANE Select	NP_000220.1:p.Lys262=