Canonical Allele Identifier: CA2661273590

Gene: LCT

Linked Data

• gnomAD v4: 2-135789869-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135789870_135789871del , CM000664.2:g.135789870_135789871del	GRCh38
NC_000002.11:g.136547440_136547441del , CM000664.1:g.136547440_136547441del	GRCh37
NC_000002.10:g.136263910_136263911del	NCBI36
NG_008104.2:g.70299_70300del , LRG_338:g.70299_70300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-73_5336-72del MANE Select	ENSP00000264162.2:n.5336-73_5336-72del
ENST00000264162.6:c.5336-73_5336-72del	ENSP00000264162.2:n.5336-73_5336-72del
NM_002299.2:c.5336-73_5336-72del , LRG_338t1:c.5336-73_5336-72del	NP_002290.2:n.5336-73_5336-72del
NM_002299.3:c.5336-73_5336-72del	NP_002290.2:n.5336-73_5336-72del
NM_002299.4:c.5336-73_5336-72del MANE Select	NP_002290.2:n.5336-73_5336-72del