Canonical Allele Identifier: CA2732690751

Gene: LCAT

Linked Data

• dbSNP Id: rs2058299312

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942778C>G , CM000678.2:g.67942778C>G	GRCh38
NC_000016.9:g.67976681C>G , CM000678.1:g.67976681C>G	GRCh37
NC_000016.8:g.66534182C>G	NCBI36
NG_009778.1:g.6335G>C
NG_033098.1:g.30917G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.428-12G>C MANE Select	ENSP00000264005.5:n.428-12G>C
ENST00000264005.9:c.428-12G>C	ENSP00000264005.5:n.428-12G>C
ENST00000570369.5:c.155+83G>C
ENST00000570980.1:c.212-12G>C	ENSP00000464651.1:n.212-12G>C
ENST00000573538.5:c.71-12G>C	ENSP00000463220.1:n.71-12G>C
ENST00000573846.1:n.42-12G>C
ENST00000575277.1:n.206-12G>C
ENST00000575467.5:c.*123-12G>C	ENSP00000460653.1:n.*123-12G>C
NM_000229.1:c.428-12G>C	NP_000220.1:n.428-12G>C
NM_000229.2:c.428-12G>C MANE Select	NP_000220.1:n.428-12G>C