Canonical Allele Identifier: CA1290822736

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135789824_135789826delinsTAA , CM000664.2:g.135789824_135789826delinsTAA	GRCh38
NC_000002.11:g.136547394_136547396delinsTAA , CM000664.1:g.136547394_136547396delinsTAA	GRCh37
NC_000002.10:g.136263864_136263866delinsTAA	NCBI36
NG_008104.2:g.70344_70346delinsTTA , LRG_338:g.70344_70346delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.5336-28_5336-26delinsTTA MANE Select	ENSP00000264162.2:n.5336-28_5336-26delinsTTA
ENST00000264162.6:c.5336-28_5336-26delinsTTA	ENSP00000264162.2:n.5336-28_5336-26delinsTTA
NM_002299.2:c.5336-28_5336-26delinsTTA , LRG_338t1:c.5336-28_5336-26delinsTTA	NP_002290.2:n.5336-28_5336-26delinsTTA
NM_002299.3:c.5336-28_5336-26delinsTTA	NP_002290.2:n.5336-28_5336-26delinsTTA
NM_002299.4:c.5336-28_5336-26delinsTTA MANE Select	NP_002290.2:n.5336-28_5336-26delinsTTA