Canonical Allele Identifier: CA1290822824

Gene: LCT

Linked Data

• dbSNP Id: rs2077521557

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135790021dup , CM000664.2:g.135790021dup	GRCh38
NC_000002.11:g.136547591dup , CM000664.1:g.136547591dup	GRCh37
NC_000002.10:g.136264061dup	NCBI36
NG_008104.2:g.70151dup , LRG_338:g.70151dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-221dup MANE Select	ENSP00000264162.2:n.5336-221dup
ENST00000264162.6:c.5336-221dup	ENSP00000264162.2:n.5336-221dup
NM_002299.2:c.5336-221dup , LRG_338t1:c.5336-221dup	NP_002290.2:n.5336-221dup
NM_002299.3:c.5336-221dup	NP_002290.2:n.5336-221dup
NM_002299.4:c.5336-221dup MANE Select	NP_002290.2:n.5336-221dup