Canonical Allele Identifier: CA2661273534
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789510_135789513del , CM000664.2:g.135789510_135789513del GRCh38
NC_000002.11:g.136547080_136547083del , CM000664.1:g.136547080_136547083del GRCh37
NC_000002.10:g.136263550_136263553del NCBI36
NG_008104.2:g.70660_70663del , LRG_338:g.70660_70663del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.5563+61_5563+64del MANE Select ENSP00000264162.2:n.5563+61_5563+64del
ENST00000264162.6:c.5563+61_5563+64del ENSP00000264162.2:n.5563+61_5563+64del
NM_002299.2:c.5563+61_5563+64del , LRG_338t1:c.5563+61_5563+64del NP_002290.2:n.5563+61_5563+64del
NM_002299.3:c.5563+61_5563+64del NP_002290.2:n.5563+61_5563+64del
NM_002299.4:c.5563+61_5563+64del MANE Select NP_002290.2:n.5563+61_5563+64del