Canonical Allele Identifier: CA2838396351

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833240dup , CM000664.2:g.135833240dup	GRCh38
NC_000002.11:g.136590810dup , CM000664.1:g.136590810dup	GRCh37
NC_000002.10:g.136307280dup	NCBI36
NG_008104.2:g.26930dup , LRG_338:g.26930dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.641-50dup MANE Select	ENSP00000264162.2:n.641-50dup
ENST00000264162.6:c.641-50dup	ENSP00000264162.2:n.641-50dup
NM_002299.2:c.641-50dup , LRG_338t1:c.641-50dup	NP_002290.2:n.641-50dup
NM_002299.3:c.641-50dup	NP_002290.2:n.641-50dup
XM_017004088.2:c.641-50dup	XP_016859577.1:n.641-50dup
NM_002299.4:c.641-50dup MANE Select	NP_002290.2:n.641-50dup