Canonical Allele Identifier: CA1290826583

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798202_135798203delinsTC , CM000664.2:g.135798202_135798203delinsTC	GRCh38
NC_000002.11:g.136555772_136555773delinsTC , CM000664.1:g.136555772_136555773delinsTC	GRCh37
NC_000002.10:g.136272242_136272243delinsTC	NCBI36
NG_008104.2:g.61967_61968delinsGA , LRG_338:g.61967_61968delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4867-65_4867-64delinsGA MANE Select	ENSP00000264162.2:n.4867-65_4867-64delinsGA
ENST00000264162.6:c.4867-65_4867-64delinsGA	ENSP00000264162.2:n.4867-65_4867-64delinsGA
ENST00000452974.1:c.2960-65_2960-64delinsGA	ENSP00000391231.1:n.2960-65_2960-64delinsGA
NM_002299.2:c.4867-65_4867-64delinsGA , LRG_338t1:c.4867-65_4867-64delinsGA	NP_002290.2:n.4867-65_4867-64delinsGA
NM_002299.3:c.4867-65_4867-64delinsGA	NP_002290.2:n.4867-65_4867-64delinsGA
XM_017004088.2:c.4867-65_4867-64delinsGA	XP_016859577.1:n.4867-65_4867-64delinsGA
NM_002299.4:c.4867-65_4867-64delinsGA MANE Select	NP_002290.2:n.4867-65_4867-64delinsGA