Canonical Allele Identifier: CA978460516
Gene: LCAT HGNC NCBI

Linked Data

gnomAD v3: 16-67940811-C-A
gnomAD v4: 16-67940811-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940811C>A , CM000678.2:g.67940811C>A GRCh38
NC_000016.9:g.67974714C>A , CM000678.1:g.67974714C>A GRCh37
NC_000016.8:g.66532215C>A NCBI36
NG_009778.1:g.8302G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.749-333G>T MANE Select ENSP00000264005.5:n.749-333G>T
ENST00000264005.9:c.749-333G>T ENSP00000264005.5:n.749-333G>T
ENST00000570369.5:c.156-737G>T
ENST00000570980.1:c.533-333G>T ENSP00000464651.1:n.533-333G>T
ENST00000573538.5:c.412G>T ENSP00000463220.1:p.Ala138Ser
NM_000229.1:c.749-333G>T NP_000220.1:n.749-333G>T
NM_000229.2:c.749-333G>T MANE Select NP_000220.1:n.749-333G>T
Search 100 bp 5'
Search 100 bp 3'