Canonical Allele Identifier: CA1290827530

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800468_135800469delinsTC , CM000664.2:g.135800468_135800469delinsTC	GRCh38
NC_000002.11:g.136558038_136558039delinsTC , CM000664.1:g.136558038_136558039delinsTC	GRCh37
NC_000002.10:g.136274508_136274509delinsTC	NCBI36
NG_008104.2:g.59701_59702delinsGA , LRG_338:g.59701_59702delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4866+138_4866+139delinsGA MANE Select	ENSP00000264162.2:n.4866+138_4866+139delinsGA
ENST00000264162.6:c.4866+138_4866+139delinsGA	ENSP00000264162.2:n.4866+138_4866+139delinsGA
ENST00000452974.1:c.2960-2331_2960-2330delinsGA	ENSP00000391231.1:n.2960-2331_2960-2330delinsGA
NM_002299.2:c.4866+138_4866+139delinsGA , LRG_338t1:c.4866+138_4866+139delinsGA	NP_002290.2:n.4866+138_4866+139delinsGA
NM_002299.3:c.4866+138_4866+139delinsGA	NP_002290.2:n.4866+138_4866+139delinsGA
XM_017004088.2:c.4866+138_4866+139delinsGA	XP_016859577.1:n.4866+138_4866+139delinsGA
NM_002299.4:c.4866+138_4866+139delinsGA MANE Select	NP_002290.2:n.4866+138_4866+139delinsGA