Canonical Allele Identifier: CA1036798900

Gene: LCT

Linked Data

• dbSNP Id: rs2077954841
• gnomAD v3: 2-135833346-A-AACACACTTCTCGGGGGATTCTGATACAGTGGTCCTCAGACC
• gnomAD v4: 2-135833346-A-AACACACTTCTCGGGGGATTCTGATACAGTGGTCCTCAGACC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135833347_135833348insCACACTTCTCGGGGGATTCTGATACAGTGGTCCTCAGACCA , CM000664.2:g.135833347_135833348insCACACTTCTCGGGGGATTCTGATACAGTGGTCCTCAGACCA	GRCh38
NC_000002.11:g.136590917_136590918insCACACTTCTCGGGGGATTCTGATACAGTGGTCCTCAGACCA , CM000664.1:g.136590917_136590918insCACACTTCTCGGGGGATTCTGATACAGTGGTCCTCAGACCA	GRCh37
NC_000002.10:g.136307387_136307388insCACACTTCTCGGGGGATTCTGATACAGTGGTCCTCAGACCA	NCBI36
NG_008104.2:g.26823_26824insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT , LRG_338:g.26823_26824insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264162.7:c.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT MANE Select	ENSP00000264162.2:n.641-157_641-156insGGTCTGAGGACCACTGTATCAGA...
ENST00000264162.6:c.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT	ENSP00000264162.2:n.641-157_641-156insGGTCTGAGGACCACTGTATCAGA...
NM_002299.2:c.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT , LRG_338t1:c.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT	NP_002290.2:n.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCC...
NM_002299.3:c.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT	NP_002290.2:n.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCC...
XM_017004088.2:c.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT	XP_016859577.1:n.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATC...
NM_002299.4:c.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCCCGAGAAGTGTGT MANE Select	NP_002290.2:n.641-157_641-156insGGTCTGAGGACCACTGTATCAGAATCCCC...