Canonical Allele Identifier: CA2513993069
Gene: LCT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787944_135787948dup , CM000664.2:g.135787944_135787948dup GRCh38
NC_000002.11:g.136545514_136545518dup , CM000664.1:g.136545514_136545518dup GRCh37
NC_000002.10:g.136261984_136261988dup NCBI36
NG_008104.2:g.72223_72227dup , LRG_338:g.72223_72227dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*377_*381dup MANE Select ENSP00000264162.2:n.*377_*381dup
ENST00000264162.6:c.*377_*381dup ENSP00000264162.2:n.*377_*381dup
NM_002299.2:c.*377_*381dup , LRG_338t1:c.*377_*381dup NP_002290.2:n.*377_*381dup
NM_002299.3:c.*377_*381dup NP_002290.2:n.*377_*381dup
NM_002299.4:c.*377_*381dup MANE Select NP_002290.2:n.*377_*381dup
Search 100 bp 5'
Search 100 bp 3'