Canonical Allele Identifier: CA1290827662

Gene: LCT

Linked Data

• dbSNP Id: rs2077620386

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135800825_135800836del , CM000664.2:g.135800825_135800836del	GRCh38
NC_000002.11:g.136558395_136558406del , CM000664.1:g.136558395_136558406del	GRCh37
NC_000002.10:g.136274865_136274876del	NCBI36
NG_008104.2:g.59337_59348del , LRG_338:g.59337_59348del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.4664-24_4664-13del MANE Select	ENSP00000264162.2:n.4664-24_4664-13del
ENST00000264162.6:c.4664-24_4664-13del	ENSP00000264162.2:n.4664-24_4664-13del
ENST00000452974.1:c.2960-2695_2960-2684del	ENSP00000391231.1:n.2960-2695_2960-2684del
NM_002299.2:c.4664-24_4664-13del , LRG_338t1:c.4664-24_4664-13del	NP_002290.2:n.4664-24_4664-13del
NM_002299.3:c.4664-24_4664-13del	NP_002290.2:n.4664-24_4664-13del
XM_017004088.2:c.4664-24_4664-13del	XP_016859577.1:n.4664-24_4664-13del
NM_002299.4:c.4664-24_4664-13del MANE Select	NP_002290.2:n.4664-24_4664-13del