Canonical Allele Identifier: CA1290821931
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787951_135787952delinsAT , CM000664.2:g.135787951_135787952delinsAT GRCh38
NC_000002.11:g.136545521_136545522delinsAT , CM000664.1:g.136545521_136545522delinsAT GRCh37
NC_000002.10:g.136261991_136261992delinsAT NCBI36
NG_008104.2:g.72218_72219delinsAT , LRG_338:g.72218_72219delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*372_*373delinsAT MANE Select ENSP00000264162.2:n.*372_*373delinsAT
ENST00000264162.6:c.*372_*373delinsAT ENSP00000264162.2:n.*372_*373delinsAT
NM_002299.2:c.*372_*373delinsAT , LRG_338t1:c.*372_*373delinsAT NP_002290.2:n.*372_*373delinsAT
NM_002299.3:c.*372_*373delinsAT NP_002290.2:n.*372_*373delinsAT
NM_002299.4:c.*372_*373delinsAT MANE Select NP_002290.2:n.*372_*373delinsAT
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