Canonical Allele Identifier: CA2752323362

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135817175_135817176insC , CM000664.2:g.135817175_135817176insC	GRCh38
NC_000002.11:g.136574745_136574746insC , CM000664.1:g.136574745_136574746insC	GRCh37
NC_000002.10:g.136291215_136291216insC	NCBI36
NG_008104.2:g.42994_42995insG , LRG_338:g.42994_42995insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.1707+165_1707+166insG MANE Select	ENSP00000264162.2:n.1707+165_1707+166insG
ENST00000264162.6:c.1707+165_1707+166insG	ENSP00000264162.2:n.1707+165_1707+166insG
NM_002299.2:c.1707+165_1707+166insG , LRG_338t1:c.1707+165_1707+166insG	NP_002290.2:n.1707+165_1707+166insG
NM_002299.3:c.1707+165_1707+166insG	NP_002290.2:n.1707+165_1707+166insG
XM_017004088.2:c.1707+165_1707+166insG	XP_016859577.1:n.1707+165_1707+166insG
NM_002299.4:c.1707+165_1707+166insG MANE Select	NP_002290.2:n.1707+165_1707+166insG