Canonical Allele Identifier: CA1036797326
Gene: LCT HGNC NCBI

Linked Data

gnomAD v3: 2-135800925-A-AT
gnomAD v4: 2-135800925-A-AT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135800925_135800926insT , CM000664.2:g.135800925_135800926insT GRCh38
NC_000002.11:g.136558495_136558496insT , CM000664.1:g.136558495_136558496insT GRCh37
NC_000002.10:g.136274965_136274966insT NCBI36
NG_008104.2:g.59244_59245insA , LRG_338:g.59244_59245insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000264162.7:c.4664-117_4664-116insA MANE Select ENSP00000264162.2:n.4664-117_4664-116insA
ENST00000264162.6:c.4664-117_4664-116insA ENSP00000264162.2:n.4664-117_4664-116insA
ENST00000452974.1:c.2960-2788_2960-2787insA ENSP00000391231.1:n.2960-2788_2960-2787insA
NM_002299.2:c.4664-117_4664-116insA , LRG_338t1:c.4664-117_4664-116insA NP_002290.2:n.4664-117_4664-116insA
NM_002299.3:c.4664-117_4664-116insA NP_002290.2:n.4664-117_4664-116insA
XM_017004088.2:c.4664-117_4664-116insA XP_016859577.1:n.4664-117_4664-116insA
NM_002299.4:c.4664-117_4664-116insA MANE Select NP_002290.2:n.4664-117_4664-116insA
Search 100 bp 5'
Search 100 bp 3'