Canonical Allele Identifier: CA2633851843

Gene: LCAT

Linked Data

• gnomAD v4: 16-67940788-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940788C>A , CM000678.2:g.67940788C>A	GRCh38
NC_000016.9:g.67974691C>A , CM000678.1:g.67974691C>A	GRCh37
NC_000016.8:g.66532192C>A	NCBI36
NG_009778.1:g.8325G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-310G>T MANE Select	ENSP00000264005.5:n.749-310G>T
ENST00000264005.9:c.749-310G>T	ENSP00000264005.5:n.749-310G>T
ENST00000570369.5:c.156-714G>T
ENST00000570980.1:c.533-310G>T	ENSP00000464651.1:n.533-310G>T
ENST00000573538.5:c.435G>T	ENSP00000463220.1:n.435G>T
NM_000229.1:c.749-310G>T	NP_000220.1:n.749-310G>T
NM_000229.2:c.749-310G>T MANE Select	NP_000220.1:n.749-310G>T