Canonical Allele Identifier: CA1887800

Gene: LCT

Linked Data

• dbSNP Id: rs771162177
• ExAC: 2:136558421 T / TGTTGCCCA
• MyVariant Identifiers: chr2:g.136558421_136558422insGTTGCCCA (hg19) ; chr2:g.135800851_135800852insGTTGCCCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800852_135800853insTTGCCCAG , CM000664.2:g.135800852_135800853insTTGCCCAG	GRCh38
NC_000002.11:g.136558422_136558423insTTGCCCAG , CM000664.1:g.136558422_136558423insTTGCCCAG	GRCh37
NC_000002.10:g.136274892_136274893insTTGCCCAG	NCBI36
NG_008104.2:g.59318_59319insTGGGCAAC , LRG_338:g.59318_59319insTGGGCAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4664-43_4664-42insTGGGCAAC MANE Select	ENSP00000264162.2:n.4664-43_4664-42insTGGGCAAC
ENST00000264162.6:c.4664-43_4664-42insTGGGCAAC	ENSP00000264162.2:n.4664-43_4664-42insTGGGCAAC
ENST00000452974.1:c.2960-2714_2960-2713insTGGGCAAC	ENSP00000391231.1:n.2960-2714_2960-2713insTGGGCAAC
NM_002299.2:c.4664-43_4664-42insTGGGCAAC , LRG_338t1:c.4664-43_4664-42insTGGGCAAC	NP_002290.2:n.4664-43_4664-42insTGGGCAAC
NM_002299.3:c.4664-43_4664-42insTGGGCAAC	NP_002290.2:n.4664-43_4664-42insTGGGCAAC
XM_017004088.2:c.4664-43_4664-42insTGGGCAAC	XP_016859577.1:n.4664-43_4664-42insTGGGCAAC
NM_002299.4:c.4664-43_4664-42insTGGGCAAC MANE Select	NP_002290.2:n.4664-43_4664-42insTGGGCAAC