Canonical Allele Identifier: CA396376311
Gene: LCAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67940418G>C , CM000678.2:g.67940418G>C GRCh38
NC_000016.9:g.67974321G>C , CM000678.1:g.67974321G>C GRCh37
NC_000016.8:g.66531822G>C NCBI36
NG_009778.1:g.8695C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264005.10:c.809C>G MANE Select ENSP00000264005.5:p.Thr270Ser
ENST00000264005.9:c.809C>G ENSP00000264005.5:p.Thr270Ser
ENST00000570369.5:c.156-344C>G
ENST00000570980.1:c.593C>G ENSP00000464651.1:p.Thr198Ser
ENST00000573538.5:c.547C>G ENSP00000463220.1:n.547C>G
NM_000229.1:c.809C>G NP_000220.1:p.Thr270Ser
NM_000229.2:c.809C>G MANE Select NP_000220.1:p.Thr270Ser