Canonical Allele Identifier: CA536394334
Gene: LCT HGNC NCBI

Linked Data

dbSNP Id: rs1257692858

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135797963_135797967del , CM000664.2:g.135797963_135797967del GRCh38
NC_000002.11:g.136555533_136555537del , CM000664.1:g.136555533_136555537del GRCh37
NC_000002.10:g.136272003_136272007del NCBI36
NG_008104.2:g.62203_62207del , LRG_338:g.62203_62207del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4976+62_4976+66del MANE Select ENSP00000264162.2:n.4976+62_4976+66del
ENST00000264162.6:c.4976+62_4976+66del ENSP00000264162.2:n.4976+62_4976+66del
ENST00000452974.1:c.3069+62_3069+66del ENSP00000391231.1:n.3069+62_3069+66del
NM_002299.2:c.4976+62_4976+66del , LRG_338t1:c.4976+62_4976+66del NP_002290.2:n.4976+62_4976+66del
NM_002299.3:c.4976+62_4976+66del NP_002290.2:n.4976+62_4976+66del
XM_017004088.2:c.4976+62_4976+66del XP_016859577.1:n.4976+62_4976+66del
NM_002299.4:c.4976+62_4976+66del MANE Select NP_002290.2:n.4976+62_4976+66del