Canonical Allele Identifier: CA2576033574

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67942786A>G , CM000678.2:g.67942786A>G	GRCh38
NC_000016.9:g.67976689A>G , CM000678.1:g.67976689A>G	GRCh37
NC_000016.8:g.66534190A>G	NCBI36
NG_009778.1:g.6327T>C
NG_033098.1:g.30909T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.428-20T>C MANE Select	ENSP00000264005.5:n.428-20T>C
ENST00000264005.9:c.428-20T>C	ENSP00000264005.5:n.428-20T>C
ENST00000570369.5:c.155+75T>C
ENST00000570980.1:c.212-20T>C	ENSP00000464651.1:n.212-20T>C
ENST00000573538.5:c.71-20T>C	ENSP00000463220.1:n.71-20T>C
ENST00000573846.1:n.42-20T>C
ENST00000575277.1:n.206-20T>C
ENST00000575467.5:c.*123-20T>C	ENSP00000460653.1:n.*123-20T>C
NM_000229.1:c.428-20T>C	NP_000220.1:n.428-20T>C
NM_000229.2:c.428-20T>C MANE Select	NP_000220.1:n.428-20T>C