Canonical Allele Identifier: CA2661275097
Gene: LCT HGNC NCBI

Linked Data

gnomAD v4: 2-135807065-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135807068del , CM000664.2:g.135807068del GRCh38
NC_000002.11:g.136564638del , CM000664.1:g.136564638del GRCh37
NC_000002.10:g.136281108del NCBI36
NG_008104.2:g.53104del , LRG_338:g.53104del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4173+62del MANE Select ENSP00000264162.2:n.4173+62del
ENST00000264162.6:c.4173+62del ENSP00000264162.2:n.4173+62del
ENST00000452974.1:c.2469+62del ENSP00000391231.1:n.2469+62del
NM_002299.2:c.4173+62del , LRG_338t1:c.4173+62del NP_002290.2:n.4173+62del
NM_002299.3:c.4173+62del NP_002290.2:n.4173+62del
XM_017004088.2:c.4173+62del XP_016859577.1:n.4173+62del
NM_002299.4:c.4173+62del MANE Select NP_002290.2:n.4173+62del
Search 100 bp 5'
Search 100 bp 3'