Canonical Allele Identifier: CA2577107636
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789556_135789560del , CM000664.2:g.135789556_135789560del GRCh38
NC_000002.11:g.136547126_136547130del , CM000664.1:g.136547126_136547130del GRCh37
NC_000002.10:g.136263596_136263600del NCBI36
NG_008104.2:g.70611_70615del , LRG_338:g.70611_70615del

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.5563+12_5563+16del MANE Select ENSP00000264162.2:n.5563+12_5563+16del
ENST00000264162.6:c.5563+12_5563+16del ENSP00000264162.2:n.5563+12_5563+16del
NM_002299.2:c.5563+12_5563+16del , LRG_338t1:c.5563+12_5563+16del NP_002290.2:n.5563+12_5563+16del
NM_002299.3:c.5563+12_5563+16del NP_002290.2:n.5563+12_5563+16del
NM_002299.4:c.5563+12_5563+16del MANE Select NP_002290.2:n.5563+12_5563+16del