Canonical Allele Identifier: CA1290822611

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135789457_135789458delinsAG , CM000664.2:g.135789457_135789458delinsAG	GRCh38
NC_000002.11:g.136547027_136547028delinsAG , CM000664.1:g.136547027_136547028delinsAG	GRCh37
NC_000002.10:g.136263497_136263498delinsAG	NCBI36
NG_008104.2:g.70712_70713delinsCT , LRG_338:g.70712_70713delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5563+113_5563+114delinsCT MANE Select	ENSP00000264162.2:n.5563+113_5563+114delinsCT
ENST00000264162.6:c.5563+113_5563+114delinsCT	ENSP00000264162.2:n.5563+113_5563+114delinsCT
NM_002299.2:c.5563+113_5563+114delinsCT , LRG_338t1:c.5563+113_5563+114delinsCT	NP_002290.2:n.5563+113_5563+114delinsCT
NM_002299.3:c.5563+113_5563+114delinsCT	NP_002290.2:n.5563+113_5563+114delinsCT
NM_002299.4:c.5563+113_5563+114delinsCT MANE Select	NP_002290.2:n.5563+113_5563+114delinsCT