Canonical Allele Identifier: CA1290826470

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135797955_135797956delinsTG , CM000664.2:g.135797955_135797956delinsTG	GRCh38
NC_000002.11:g.136555525_136555526delinsTG , CM000664.1:g.136555525_136555526delinsTG	GRCh37
NC_000002.10:g.136271995_136271996delinsTG	NCBI36
NG_008104.2:g.62214_62215delinsCA , LRG_338:g.62214_62215delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4976+73_4976+74delinsCA MANE Select	ENSP00000264162.2:n.4976+73_4976+74delinsCA
ENST00000264162.6:c.4976+73_4976+74delinsCA	ENSP00000264162.2:n.4976+73_4976+74delinsCA
ENST00000452974.1:c.3069+73_3069+74delinsCA	ENSP00000391231.1:n.3069+73_3069+74delinsCA
NM_002299.2:c.4976+73_4976+74delinsCA , LRG_338t1:c.4976+73_4976+74delinsCA	NP_002290.2:n.4976+73_4976+74delinsCA
NM_002299.3:c.4976+73_4976+74delinsCA	NP_002290.2:n.4976+73_4976+74delinsCA
XM_017004088.2:c.4976+73_4976+74delinsCA	XP_016859577.1:n.4976+73_4976+74delinsCA
NM_002299.4:c.4976+73_4976+74delinsCA MANE Select	NP_002290.2:n.4976+73_4976+74delinsCA