Canonical Allele Identifier: CA1290827690

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800889_135800890delinsTC , CM000664.2:g.135800889_135800890delinsTC	GRCh38
NC_000002.11:g.136558459_136558460delinsTC , CM000664.1:g.136558459_136558460delinsTC	GRCh37
NC_000002.10:g.136274929_136274930delinsTC	NCBI36
NG_008104.2:g.59280_59281delinsGA , LRG_338:g.59280_59281delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4664-81_4664-80delinsGA MANE Select	ENSP00000264162.2:n.4664-81_4664-80delinsGA
ENST00000264162.6:c.4664-81_4664-80delinsGA	ENSP00000264162.2:n.4664-81_4664-80delinsGA
ENST00000452974.1:c.2960-2752_2960-2751delinsGA	ENSP00000391231.1:n.2960-2752_2960-2751delinsGA
NM_002299.2:c.4664-81_4664-80delinsGA , LRG_338t1:c.4664-81_4664-80delinsGA	NP_002290.2:n.4664-81_4664-80delinsGA
NM_002299.3:c.4664-81_4664-80delinsGA	NP_002290.2:n.4664-81_4664-80delinsGA
XM_017004088.2:c.4664-81_4664-80delinsGA	XP_016859577.1:n.4664-81_4664-80delinsGA
NM_002299.4:c.4664-81_4664-80delinsGA MANE Select	NP_002290.2:n.4664-81_4664-80delinsGA