Canonical Allele Identifier: CA1290826575

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135798193_135798196delinsACAG , CM000664.2:g.135798193_135798196delinsACAG	GRCh38
NC_000002.11:g.136555763_136555766delinsACAG , CM000664.1:g.136555763_136555766delinsACAG	GRCh37
NC_000002.10:g.136272233_136272236delinsACAG	NCBI36
NG_008104.2:g.61974_61977delinsCTGT , LRG_338:g.61974_61977delinsCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4867-58_4867-55delinsCTGT MANE Select	ENSP00000264162.2:n.4867-58_4867-55delinsCTGT
ENST00000264162.6:c.4867-58_4867-55delinsCTGT	ENSP00000264162.2:n.4867-58_4867-55delinsCTGT
ENST00000452974.1:c.2960-58_2960-55delinsCTGT	ENSP00000391231.1:n.2960-58_2960-55delinsCTGT
NM_002299.2:c.4867-58_4867-55delinsCTGT , LRG_338t1:c.4867-58_4867-55delinsCTGT	NP_002290.2:n.4867-58_4867-55delinsCTGT
NM_002299.3:c.4867-58_4867-55delinsCTGT	NP_002290.2:n.4867-58_4867-55delinsCTGT
XM_017004088.2:c.4867-58_4867-55delinsCTGT	XP_016859577.1:n.4867-58_4867-55delinsCTGT
NM_002299.4:c.4867-58_4867-55delinsCTGT MANE Select	NP_002290.2:n.4867-58_4867-55delinsCTGT