Canonical Allele Identifier: CA1290826434

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135797860_135797861delinsAC , CM000664.2:g.135797860_135797861delinsAC	GRCh38
NC_000002.11:g.136555430_136555431delinsAC , CM000664.1:g.136555430_136555431delinsAC	GRCh37
NC_000002.10:g.136271900_136271901delinsAC	NCBI36
NG_008104.2:g.62309_62310delinsGT , LRG_338:g.62309_62310delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000264162.7:c.4976+168_4976+169delinsGT MANE Select	ENSP00000264162.2:n.4976+168_4976+169delinsGT
ENST00000264162.6:c.4976+168_4976+169delinsGT	ENSP00000264162.2:n.4976+168_4976+169delinsGT
ENST00000452974.1:c.3069+168_3069+169delinsGT	ENSP00000391231.1:n.3069+168_3069+169delinsGT
NM_002299.2:c.4976+168_4976+169delinsGT , LRG_338t1:c.4976+168_4976+169delinsGT	NP_002290.2:n.4976+168_4976+169delinsGT
NM_002299.3:c.4976+168_4976+169delinsGT	NP_002290.2:n.4976+168_4976+169delinsGT
XM_017004088.2:c.4976+168_4976+169delinsGT	XP_016859577.1:n.4976+168_4976+169delinsGT
NM_002299.4:c.4976+168_4976+169delinsGT MANE Select	NP_002290.2:n.4976+168_4976+169delinsGT