Canonical Allele Identifier: CA2752308376

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798189_135798190insAACACCAAACACACCC , CM000664.2:g.135798189_135798190insAACACCAAACACACCC	GRCh38
NC_000002.11:g.136555759_136555760insAACACCAAACACACCC , CM000664.1:g.136555759_136555760insAACACCAAACACACCC	GRCh37
NC_000002.10:g.136272229_136272230insAACACCAAACACACCC	NCBI36
NG_008104.2:g.61980_61981insGGGTGTGTTTGGTGTT , LRG_338:g.61980_61981insGGGTGTGTTTGGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4867-52_4867-51insGGGTGTGTTTGGTGTT MANE Select	ENSP00000264162.2:n.4867-52_4867-51insGGGTGTGTTTGGTGTT
ENST00000264162.6:c.4867-52_4867-51insGGGTGTGTTTGGTGTT	ENSP00000264162.2:n.4867-52_4867-51insGGGTGTGTTTGGTGTT
ENST00000452974.1:c.2960-52_2960-51insGGGTGTGTTTGGTGTT	ENSP00000391231.1:n.2960-52_2960-51insGGGTGTGTTTGGTGTT
NM_002299.2:c.4867-52_4867-51insGGGTGTGTTTGGTGTT , LRG_338t1:c.4867-52_4867-51insGGGTGTGTTTGGTGTT	NP_002290.2:n.4867-52_4867-51insGGGTGTGTTTGGTGTT
NM_002299.3:c.4867-52_4867-51insGGGTGTGTTTGGTGTT	NP_002290.2:n.4867-52_4867-51insGGGTGTGTTTGGTGTT
XM_017004088.2:c.4867-52_4867-51insGGGTGTGTTTGGTGTT	XP_016859577.1:n.4867-52_4867-51insGGGTGTGTTTGGTGTT
NM_002299.4:c.4867-52_4867-51insGGGTGTGTTTGGTGTT MANE Select	NP_002290.2:n.4867-52_4867-51insGGGTGTGTTTGGTGTT