Canonical Allele Identifier: CA2661273571

Gene: LCT

Linked Data

• gnomAD v4: 2-135789810-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135789813_135789814del , CM000664.2:g.135789813_135789814del	GRCh38
NC_000002.11:g.136547383_136547384del , CM000664.1:g.136547383_136547384del	GRCh37
NC_000002.10:g.136263853_136263854del	NCBI36
NG_008104.2:g.70358_70359del , LRG_338:g.70358_70359del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-14_5336-13del MANE Select	ENSP00000264162.2:n.5336-14_5336-13del
ENST00000264162.6:c.5336-14_5336-13del	ENSP00000264162.2:n.5336-14_5336-13del
NM_002299.2:c.5336-14_5336-13del , LRG_338t1:c.5336-14_5336-13del	NP_002290.2:n.5336-14_5336-13del
NM_002299.3:c.5336-14_5336-13del	NP_002290.2:n.5336-14_5336-13del
NM_002299.4:c.5336-14_5336-13del MANE Select	NP_002290.2:n.5336-14_5336-13del