Canonical Allele Identifier: CA1290834634

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135817043_135817044delinsAT , CM000664.2:g.135817043_135817044delinsAT	GRCh38
NC_000002.11:g.136574613_136574614delinsAT , CM000664.1:g.136574613_136574614delinsAT	GRCh37
NC_000002.10:g.136291083_136291084delinsAT	NCBI36
NG_008104.2:g.43126_43127delinsAT , LRG_338:g.43126_43127delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.1707+297_1707+298delinsAT MANE Select	ENSP00000264162.2:n.1707+297_1707+298delinsAT
ENST00000264162.6:c.1707+297_1707+298delinsAT	ENSP00000264162.2:n.1707+297_1707+298delinsAT
NM_002299.2:c.1707+297_1707+298delinsAT , LRG_338t1:c.1707+297_1707+298delinsAT	NP_002290.2:n.1707+297_1707+298delinsAT
NM_002299.3:c.1707+297_1707+298delinsAT	NP_002290.2:n.1707+297_1707+298delinsAT
XM_017004088.2:c.1707+297_1707+298delinsAT	XP_016859577.1:n.1707+297_1707+298delinsAT
NM_002299.4:c.1707+297_1707+298delinsAT MANE Select	NP_002290.2:n.1707+297_1707+298delinsAT