Canonical Allele Identifier: CA2229564537

Gene: LCAT

Linked Data

• dbSNP Id: rs2058299277
• gnomAD v4: 16-67942777-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942777A>C , CM000678.2:g.67942777A>C	GRCh38
NC_000016.9:g.67976680A>C , CM000678.1:g.67976680A>C	GRCh37
NC_000016.8:g.66534181A>C	NCBI36
NG_009778.1:g.6336T>G
NG_033098.1:g.30918T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.428-11T>G MANE Select	ENSP00000264005.5:n.428-11T>G
ENST00000264005.9:c.428-11T>G	ENSP00000264005.5:n.428-11T>G
ENST00000570369.5:c.155+84T>G
ENST00000570980.1:c.212-11T>G	ENSP00000464651.1:n.212-11T>G
ENST00000573538.5:c.71-11T>G	ENSP00000463220.1:n.71-11T>G
ENST00000573846.1:n.42-11T>G
ENST00000575277.1:n.206-11T>G
ENST00000575467.5:c.*123-11T>G	ENSP00000460653.1:n.*123-11T>G
NM_000229.1:c.428-11T>G	NP_000220.1:n.428-11T>G
NM_000229.2:c.428-11T>G MANE Select	NP_000220.1:n.428-11T>G