Canonical Allele Identifier: CA1290821925
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787932A= , CM000664.2:g.135787932A= GRCh38
NC_000002.11:g.136545502A= , CM000664.1:g.136545502A= GRCh37
NC_000002.10:g.136261972A= NCBI36
NG_008104.2:g.72238T= , LRG_338:g.72238T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*392T= MANE Select ENSP00000264162.2:n.*392T=
ENST00000264162.6:c.*392T= ENSP00000264162.2:n.*392T=
NM_002299.2:c.*392T= , LRG_338t1:c.*392T= NP_002290.2:n.*392T=
NM_002299.3:c.*392T= NP_002290.2:n.*392T=
NM_002299.4:c.*392T= MANE Select NP_002290.2:n.*392T=