Canonical Allele Identifier: CA348605622
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817366G>T , CM000664.2:g.135817366G>T GRCh38
NC_000002.11:g.136574936G>T , CM000664.1:g.136574936G>T GRCh37
NC_000002.10:g.136291406G>T NCBI36
NG_008104.2:g.42804C>A , LRG_338:g.42804C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.1682C>A MANE Select ENSP00000264162.2:p.Ser561Tyr
ENST00000264162.6:c.1682C>A ENSP00000264162.2:p.Ser561Tyr
NM_002299.2:c.1682C>A , LRG_338t1:c.1682C>A NP_002290.2:p.Ser561Tyr
NM_002299.3:c.1682C>A NP_002290.2:p.Ser561Tyr
XM_017004088.2:c.1682C>A XP_016859577.1:p.Ser561Tyr
NM_002299.4:c.1682C>A MANE Select NP_002290.2:p.Ser561Tyr