Canonical Allele Identifier: CA1290821918
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787910G= , CM000664.2:g.135787910G= GRCh38
NC_000002.11:g.136545480G= , CM000664.1:g.136545480G= GRCh37
NC_000002.10:g.136261950G= NCBI36
NG_008104.2:g.72260C= , LRG_338:g.72260C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*414C= MANE Select ENSP00000264162.2:n.*414C=
ENST00000264162.6:c.*414C= ENSP00000264162.2:n.*414C=
NM_002299.2:c.*414C= , LRG_338t1:c.*414C= NP_002290.2:n.*414C=
NM_002299.3:c.*414C= NP_002290.2:n.*414C=
NM_002299.4:c.*414C= MANE Select NP_002290.2:n.*414C=