Canonical Allele Identifier: CA1290822807

Gene: LCT

Linked Data

• dbSNP Id: rs2077521352

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135789989del , CM000664.2:g.135789989del	GRCh38
NC_000002.11:g.136547559del , CM000664.1:g.136547559del	GRCh37
NC_000002.10:g.136264029del	NCBI36
NG_008104.2:g.70181del , LRG_338:g.70181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-191del MANE Select	ENSP00000264162.2:n.5336-191del
ENST00000264162.6:c.5336-191del	ENSP00000264162.2:n.5336-191del
NM_002299.2:c.5336-191del , LRG_338t1:c.5336-191del	NP_002290.2:n.5336-191del
NM_002299.3:c.5336-191del	NP_002290.2:n.5336-191del
NM_002299.4:c.5336-191del MANE Select	NP_002290.2:n.5336-191del