Canonical Allele Identifier: CA1290822614
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789464G= , CM000664.2:g.135789464G= GRCh38
NC_000002.11:g.136547034G= , CM000664.1:g.136547034G= GRCh37
NC_000002.10:g.136263504G= NCBI36
NG_008104.2:g.70706C= , LRG_338:g.70706C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.5563+107C= MANE Select ENSP00000264162.2:n.5563+107C=
ENST00000264162.6:c.5563+107C= ENSP00000264162.2:n.5563+107C=
NM_002299.2:c.5563+107C= , LRG_338t1:c.5563+107C= NP_002290.2:n.5563+107C=
NM_002299.3:c.5563+107C= NP_002290.2:n.5563+107C=
NM_002299.4:c.5563+107C= MANE Select NP_002290.2:n.5563+107C=