Canonical Allele Identifier: CA1036793656
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135790042_135790043insTTTTAATGATA , CM000664.2:g.135790042_135790043insTTTTAATGATA GRCh38
NC_000002.11:g.136547612_136547613insTTTTAATGATA , CM000664.1:g.136547612_136547613insTTTTAATGATA GRCh37
NC_000002.10:g.136264082_136264083insTTTTAATGATA NCBI36
NG_008104.2:g.70127_70128insTATCATTAAAA , LRG_338:g.70127_70128insTATCATTAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.5336-245_5336-244insTATCATTAAAA MANE Select ENSP00000264162.2:n.5336-245_5336-244insTATCATTAAAA
ENST00000264162.6:c.5336-245_5336-244insTATCATTAAAA ENSP00000264162.2:n.5336-245_5336-244insTATCATTAAAA
NM_002299.2:c.5336-245_5336-244insTATCATTAAAA , LRG_338t1:c.5336-245_5336-244insTATCATTAAAA NP_002290.2:n.5336-245_5336-244insTATCATTAAAA
NM_002299.3:c.5336-245_5336-244insTATCATTAAAA NP_002290.2:n.5336-245_5336-244insTATCATTAAAA
NM_002299.4:c.5336-245_5336-244insTATCATTAAAA MANE Select NP_002290.2:n.5336-245_5336-244insTATCATTAAAA