Canonical Allele Identifier: CA1290822836

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135790043_135790044delinsCG , CM000664.2:g.135790043_135790044delinsCG	GRCh38
NC_000002.11:g.136547613_136547614delinsCG , CM000664.1:g.136547613_136547614delinsCG	GRCh37
NC_000002.10:g.136264083_136264084delinsCG	NCBI36
NG_008104.2:g.70126_70127delinsCG , LRG_338:g.70126_70127delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-246_5336-245delinsCG MANE Select	ENSP00000264162.2:n.5336-246_5336-245delinsCG
ENST00000264162.6:c.5336-246_5336-245delinsCG	ENSP00000264162.2:n.5336-246_5336-245delinsCG
NM_002299.2:c.5336-246_5336-245delinsCG , LRG_338t1:c.5336-246_5336-245delinsCG	NP_002290.2:n.5336-246_5336-245delinsCG
NM_002299.3:c.5336-246_5336-245delinsCG	NP_002290.2:n.5336-246_5336-245delinsCG
NM_002299.4:c.5336-246_5336-245delinsCG MANE Select	NP_002290.2:n.5336-246_5336-245delinsCG