Canonical Allele Identifier: CA1036797324

Gene: LCT

Linked Data

• gnomAD v3: 2-135800922-C-CGG
• gnomAD v4: 2-135800922-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800922_135800923insGG , CM000664.2:g.135800922_135800923insGG	GRCh38
NC_000002.11:g.136558492_136558493insGG , CM000664.1:g.136558492_136558493insGG	GRCh37
NC_000002.10:g.136274962_136274963insGG	NCBI36
NG_008104.2:g.59247_59248insCC , LRG_338:g.59247_59248insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4664-114_4664-113insCC MANE Select	ENSP00000264162.2:n.4664-114_4664-113insCC
ENST00000264162.6:c.4664-114_4664-113insCC	ENSP00000264162.2:n.4664-114_4664-113insCC
ENST00000452974.1:c.2960-2785_2960-2784insCC	ENSP00000391231.1:n.2960-2785_2960-2784insCC
NM_002299.2:c.4664-114_4664-113insCC , LRG_338t1:c.4664-114_4664-113insCC	NP_002290.2:n.4664-114_4664-113insCC
NM_002299.3:c.4664-114_4664-113insCC	NP_002290.2:n.4664-114_4664-113insCC
XM_017004088.2:c.4664-114_4664-113insCC	XP_016859577.1:n.4664-114_4664-113insCC
NM_002299.4:c.4664-114_4664-113insCC MANE Select	NP_002290.2:n.4664-114_4664-113insCC