Canonical Allele Identifier: CA1036793072
Gene: LCT HGNC NCBI

Linked Data

gnomAD v3: 2-135788058-CCACTAG-C
gnomAD v4: 2-135788058-CCACTAG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135788059_135788064del , CM000664.2:g.135788059_135788064del GRCh38
NC_000002.11:g.136545629_136545634del , CM000664.1:g.136545629_136545634del GRCh37
NC_000002.10:g.136262099_136262104del NCBI36
NG_008104.2:g.72106_72111del , LRG_338:g.72106_72111del

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.*260_*265del MANE Select ENSP00000264162.2:n.*260_*265del
ENST00000264162.6:c.*260_*265del ENSP00000264162.2:n.*260_*265del
NM_002299.2:c.*260_*265del , LRG_338t1:c.*260_*265del NP_002290.2:n.*260_*265del
NM_002299.3:c.*260_*265del NP_002290.2:n.*260_*265del
NM_002299.4:c.*260_*265del MANE Select NP_002290.2:n.*260_*265del
Search 100 bp 5'
Search 100 bp 3'