Canonical Allele Identifier: CA645531704
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135817349_135817357del , CM000664.2:g.135817349_135817357del GRCh38
NC_000002.11:g.136574919_136574927del , CM000664.1:g.136574919_136574927del GRCh37
NC_000002.10:g.136291389_136291397del NCBI36
NG_008104.2:g.42813_42821del , LRG_338:g.42813_42821del

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.1691_1699del MANE Select ENSP00000264162.2:p.Gly564_Ser567delinsAl...
ENST00000264162.6:c.1691_1699del ENSP00000264162.2:p.Gly564_Ser567delinsAl...
NM_002299.2:c.1691_1699del , LRG_338t1:c.1691_1699del NP_002290.2:p.Gly564_Ser567delinsAla
NM_002299.3:c.1691_1699del NP_002290.2:p.Gly564_Ser567delinsAla
XM_017004088.2:c.1691_1699del XP_016859577.1:p.Gly564_Ser567delinsAla
NM_002299.4:c.1691_1699del MANE Select NP_002290.2:p.Gly564_Ser567delinsAla