Canonical Allele Identifier: CA2229564546

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942787C= , CM000678.2:g.67942787C=	GRCh38
NC_000016.9:g.67976690C= , CM000678.1:g.67976690C=	GRCh37
NC_000016.8:g.66534191C=	NCBI36
NG_009778.1:g.6326G=
NG_033098.1:g.30908G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264005.10:c.428-21G= MANE Select	ENSP00000264005.5:n.428-21G=
ENST00000264005.9:c.428-21G=	ENSP00000264005.5:n.428-21G=
ENST00000570369.5:c.155+74G=
ENST00000570980.1:c.212-21G=	ENSP00000464651.1:n.212-21G=
ENST00000573538.5:c.71-21G=	ENSP00000463220.1:n.71-21G=
ENST00000573846.1:n.42-21G=
ENST00000575277.1:n.206-21G=
ENST00000575467.5:c.*123-21G=	ENSP00000460653.1:n.*123-21G=
NM_000229.1:c.428-21G=	NP_000220.1:n.428-21G=
NM_000229.2:c.428-21G= MANE Select	NP_000220.1:n.428-21G=