Canonical Allele Identifier: CA1290834745
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817351_135817356delinsGCCACT , CM000664.2:g.135817351_135817356delinsGCCACT GRCh38
NC_000002.11:g.136574921_136574926delinsGCCACT , CM000664.1:g.136574921_136574926delinsGCCACT GRCh37
NC_000002.10:g.136291391_136291396delinsGCCACT NCBI36
NG_008104.2:g.42814_42819delinsAGTGGC , LRG_338:g.42814_42819delinsAGTGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.1692_1697delinsAGTGGC MANE Select ENSP00000264162.2:p.Gly564=
ENST00000264162.6:c.1692_1697delinsAGTGGC ENSP00000264162.2:p.Gly564=
NM_002299.2:c.1692_1697delinsAGTGGC , LRG_338t1:c.1692_1697delinsAGTGGC NP_002290.2:p.Gly564=
NM_002299.3:c.1692_1697delinsAGTGGC NP_002290.2:p.Gly564=
XM_017004088.2:c.1692_1697delinsAGTGGC XP_016859577.1:p.Gly564=
NM_002299.4:c.1692_1697delinsAGTGGC MANE Select NP_002290.2:p.Gly564=