Canonical Allele Identifier: CA2577108108
Gene: LCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135833097del , CM000664.2:g.135833097del GRCh38
NC_000002.11:g.136590667del , CM000664.1:g.136590667del GRCh37
NC_000002.10:g.136307137del NCBI36
NG_008104.2:g.27077del , LRG_338:g.27077del

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.720+18del MANE Select ENSP00000264162.2:n.720+18del
ENST00000264162.6:c.720+18del ENSP00000264162.2:n.720+18del
NM_002299.2:c.720+18del , LRG_338t1:c.720+18del NP_002290.2:n.720+18del
NM_002299.3:c.720+18del NP_002290.2:n.720+18del
XM_017004088.2:c.720+18del XP_016859577.1:n.720+18del
NM_002299.4:c.720+18del MANE Select NP_002290.2:n.720+18del