Canonical Allele Identifier: CA1036793652

Gene: LCT

Linked Data

• gnomAD v3: 2-135790036-TGGGAG-T
• gnomAD v4: 2-135790036-TGGGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135790037_135790041del , CM000664.2:g.135790037_135790041del	GRCh38
NC_000002.11:g.136547607_136547611del , CM000664.1:g.136547607_136547611del	GRCh37
NC_000002.10:g.136264077_136264081del	NCBI36
NG_008104.2:g.70129_70133del , LRG_338:g.70129_70133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-243_5336-239del MANE Select	ENSP00000264162.2:n.5336-243_5336-239del
ENST00000264162.6:c.5336-243_5336-239del	ENSP00000264162.2:n.5336-243_5336-239del
NM_002299.2:c.5336-243_5336-239del , LRG_338t1:c.5336-243_5336-239del	NP_002290.2:n.5336-243_5336-239del
NM_002299.3:c.5336-243_5336-239del	NP_002290.2:n.5336-243_5336-239del
NM_002299.4:c.5336-243_5336-239del MANE Select	NP_002290.2:n.5336-243_5336-239del