Canonical Allele Identifier: CA2633848137

Gene: LCAT

Linked Data

• gnomAD v4: 16-67942787-C-T

Genomic Alleles

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

Transcript Alleles

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