Canonical Allele Identifier: CA2576033454

Gene: LCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67940502A>C , CM000678.2:g.67940502A>C	GRCh38
NC_000016.9:g.67974405A>C , CM000678.1:g.67974405A>C	GRCh37
NC_000016.8:g.66531906A>C	NCBI36
NG_009778.1:g.8611T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264005.10:c.749-24T>G MANE Select	ENSP00000264005.5:n.749-24T>G
ENST00000264005.9:c.749-24T>G	ENSP00000264005.5:n.749-24T>G
ENST00000570369.5:c.156-428T>G
ENST00000570980.1:c.533-24T>G	ENSP00000464651.1:n.533-24T>G
ENST00000573538.5:c.487-24T>G	ENSP00000463220.1:n.487-24T>G
NM_000229.1:c.749-24T>G	NP_000220.1:n.749-24T>G
NM_000229.2:c.749-24T>G MANE Select	NP_000220.1:n.749-24T>G