Canonical Allele Identifier: CA1290822681
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135789651G= , CM000664.2:g.135789651G= GRCh38
NC_000002.11:g.136547221G= , CM000664.1:g.136547221G= GRCh37
NC_000002.10:g.136263691G= NCBI36
NG_008104.2:g.70519C= , LRG_338:g.70519C=

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.5483C= MANE Select ENSP00000264162.2:p.Ala1828=
ENST00000264162.6:c.5483C= ENSP00000264162.2:p.Ala1828=
NM_002299.2:c.5483C= , LRG_338t1:c.5483C= NP_002290.2:p.Ala1828=
NM_002299.3:c.5483C= NP_002290.2:p.Ala1828=
NM_002299.4:c.5483C= MANE Select NP_002290.2:p.Ala1828=