Canonical Allele Identifier: CA2661276674

Gene: LCT

Linked Data

• gnomAD v4: 2-135833064-T-TCAAACTC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833065_135833071dup , CM000664.2:g.135833065_135833071dup	GRCh38
NC_000002.11:g.136590635_136590641dup , CM000664.1:g.136590635_136590641dup	GRCh37
NC_000002.10:g.136307105_136307111dup	NCBI36
NG_008104.2:g.27099_27105dup , LRG_338:g.27099_27105dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.720+40_720+46dup MANE Select	ENSP00000264162.2:n.720+40_720+46dup
ENST00000264162.6:c.720+40_720+46dup	ENSP00000264162.2:n.720+40_720+46dup
NM_002299.2:c.720+40_720+46dup , LRG_338t1:c.720+40_720+46dup	NP_002290.2:n.720+40_720+46dup
NM_002299.3:c.720+40_720+46dup	NP_002290.2:n.720+40_720+46dup
XM_017004088.2:c.720+40_720+46dup	XP_016859577.1:n.720+40_720+46dup
NM_002299.4:c.720+40_720+46dup MANE Select	NP_002290.2:n.720+40_720+46dup