Canonical Allele Identifier: CA1290821955

Gene: LCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135787987_135787997delinsTCCCTTAACAA , CM000664.2:g.135787987_135787997delinsTCCCTTAACAA	GRCh38
NC_000002.11:g.136545557_136545567delinsTCCCTTAACAA , CM000664.1:g.136545557_136545567delinsTCCCTTAACAA	GRCh37
NC_000002.10:g.136262027_136262037delinsTCCCTTAACAA	NCBI36
NG_008104.2:g.72173_72183delinsTTGTTAAGGGA , LRG_338:g.72173_72183delinsTTGTTAAGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.*327_*337delinsTTGTTAAGGGA MANE Select	ENSP00000264162.2:n.*327_*337delinsTTGTTAAGGGA
ENST00000264162.6:c.*327_*337delinsTTGTTAAGGGA	ENSP00000264162.2:n.*327_*337delinsTTGTTAAGGGA
NM_002299.2:c.*327_*337delinsTTGTTAAGGGA , LRG_338t1:c.*327_*337delinsTTGTTAAGGGA	NP_002290.2:n.*327_*337delinsTTGTTAAGGGA
NM_002299.3:c.*327_*337delinsTTGTTAAGGGA	NP_002290.2:n.*327_*337delinsTTGTTAAGGGA
NM_002299.4:c.*327_*337delinsTTGTTAAGGGA MANE Select	NP_002290.2:n.*327_*337delinsTTGTTAAGGGA