Canonical Allele Identifier: CA1290821927
Gene: LCT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787938T= , CM000664.2:g.135787938T= GRCh38
NC_000002.11:g.136545508T= , CM000664.1:g.136545508T= GRCh37
NC_000002.10:g.136261978T= NCBI36
NG_008104.2:g.72232A= , LRG_338:g.72232A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*386A= MANE Select ENSP00000264162.2:n.*386A=
ENST00000264162.6:c.*386A= ENSP00000264162.2:n.*386A=
NM_002299.2:c.*386A= , LRG_338t1:c.*386A= NP_002290.2:n.*386A=
NM_002299.3:c.*386A= NP_002290.2:n.*386A=
NM_002299.4:c.*386A= MANE Select NP_002290.2:n.*386A=
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