Canonical Allele Identifier: CA1290822814

Gene: LCT

Linked Data

• dbSNP Id: rs2077521428

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135790006_135790008dup , CM000664.2:g.135790006_135790008dup	GRCh38
NC_000002.11:g.136547576_136547578dup , CM000664.1:g.136547576_136547578dup	GRCh37
NC_000002.10:g.136264046_136264048dup	NCBI36
NG_008104.2:g.70165_70167dup , LRG_338:g.70165_70167dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-207_5336-205dup MANE Select	ENSP00000264162.2:n.5336-207_5336-205dup
ENST00000264162.6:c.5336-207_5336-205dup	ENSP00000264162.2:n.5336-207_5336-205dup
NM_002299.2:c.5336-207_5336-205dup , LRG_338t1:c.5336-207_5336-205dup	NP_002290.2:n.5336-207_5336-205dup
NM_002299.3:c.5336-207_5336-205dup	NP_002290.2:n.5336-207_5336-205dup
NM_002299.4:c.5336-207_5336-205dup MANE Select	NP_002290.2:n.5336-207_5336-205dup