Canonical Allele Identifier: CA2661271150

Gene: LCT

Linked Data

• gnomAD v4: 2-135787942-ATGGAGTTGATTTCTTCTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135787943_135787960del , CM000664.2:g.135787943_135787960del	GRCh38
NC_000002.11:g.136545513_136545530del , CM000664.1:g.136545513_136545530del	GRCh37
NC_000002.10:g.136261983_136262000del	NCBI36
NG_008104.2:g.72210_72227del , LRG_338:g.72210_72227del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.*364_*381del MANE Select	ENSP00000264162.2:n.*364_*381del
ENST00000264162.6:c.*364_*381del	ENSP00000264162.2:n.*364_*381del
NM_002299.2:c.*364_*381del , LRG_338t1:c.*364_*381del	NP_002290.2:n.*364_*381del
NM_002299.3:c.*364_*381del	NP_002290.2:n.*364_*381del
NM_002299.4:c.*364_*381del MANE Select	NP_002290.2:n.*364_*381del