Canonical Allele Identifier: CA1290822019
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788139_135788140delinsTG , CM000664.2:g.135788139_135788140delinsTG GRCh38
NC_000002.11:g.136545709_136545710delinsTG , CM000664.1:g.136545709_136545710delinsTG GRCh37
NC_000002.10:g.136262179_136262180delinsTG NCBI36
NG_008104.2:g.72030_72031delinsCA , LRG_338:g.72030_72031delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*184_*185delinsCA MANE Select ENSP00000264162.2:n.*184_*185delinsCA
ENST00000264162.6:c.*184_*185delinsCA ENSP00000264162.2:n.*184_*185delinsCA
NM_002299.2:c.*184_*185delinsCA , LRG_338t1:c.*184_*185delinsCA NP_002290.2:n.*184_*185delinsCA
NM_002299.3:c.*184_*185delinsCA NP_002290.2:n.*184_*185delinsCA
NM_002299.4:c.*184_*185delinsCA MANE Select NP_002290.2:n.*184_*185delinsCA
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