Canonical Allele Identifier: CA1290826612

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798249_135798250delinsAC , CM000664.2:g.135798249_135798250delinsAC	GRCh38
NC_000002.11:g.136555819_136555820delinsAC , CM000664.1:g.136555819_136555820delinsAC	GRCh37
NC_000002.10:g.136272289_136272290delinsAC	NCBI36
NG_008104.2:g.61920_61921delinsGT , LRG_338:g.61920_61921delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4867-112_4867-111delinsGT MANE Select	ENSP00000264162.2:n.4867-112_4867-111delinsGT
ENST00000264162.6:c.4867-112_4867-111delinsGT	ENSP00000264162.2:n.4867-112_4867-111delinsGT
ENST00000452974.1:c.2960-112_2960-111delinsGT	ENSP00000391231.1:n.2960-112_2960-111delinsGT
NM_002299.2:c.4867-112_4867-111delinsGT , LRG_338t1:c.4867-112_4867-111delinsGT	NP_002290.2:n.4867-112_4867-111delinsGT
NM_002299.3:c.4867-112_4867-111delinsGT	NP_002290.2:n.4867-112_4867-111delinsGT
XM_017004088.2:c.4867-112_4867-111delinsGT	XP_016859577.1:n.4867-112_4867-111delinsGT
NM_002299.4:c.4867-112_4867-111delinsGT MANE Select	NP_002290.2:n.4867-112_4867-111delinsGT