Canonical Allele Identifier: CA1290822017
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788135_135788141delinsAAGATGG , CM000664.2:g.135788135_135788141delinsAAGATGG GRCh38
NC_000002.11:g.136545705_136545711delinsAAGATGG , CM000664.1:g.136545705_136545711delinsAAGATGG GRCh37
NC_000002.10:g.136262175_136262181delinsAAGATGG NCBI36
NG_008104.2:g.72029_72035delinsCCATCTT , LRG_338:g.72029_72035delinsCCATCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.*183_*189delinsCCATCTT MANE Select ENSP00000264162.2:n.*183_*189delinsCCATCTT
ENST00000264162.6:c.*183_*189delinsCCATCTT ENSP00000264162.2:n.*183_*189delinsCCATCTT
NM_002299.2:c.*183_*189delinsCCATCTT , LRG_338t1:c.*183_*189delinsCCATCTT NP_002290.2:n.*183_*189delinsCCATCTT
NM_002299.3:c.*183_*189delinsCCATCTT NP_002290.2:n.*183_*189delinsCCATCTT
NM_002299.4:c.*183_*189delinsCCATCTT MANE Select NP_002290.2:n.*183_*189delinsCCATCTT
Search 100 bp 5'
Search 100 bp 3'