Canonical Allele Identifier: CA1290821935
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135787955C= , CM000664.2:g.135787955C= GRCh38
NC_000002.11:g.136545525C= , CM000664.1:g.136545525C= GRCh37
NC_000002.10:g.136261995C= NCBI36
NG_008104.2:g.72215G= , LRG_338:g.72215G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.*369G= MANE Select ENSP00000264162.2:n.*369G=
ENST00000264162.6:c.*369G= ENSP00000264162.2:n.*369G=
NM_002299.2:c.*369G= , LRG_338t1:c.*369G= NP_002290.2:n.*369G=
NM_002299.3:c.*369G= NP_002290.2:n.*369G=
NM_002299.4:c.*369G= MANE Select NP_002290.2:n.*369G=