Canonical Allele Identifier: CA1290826505
Gene: LCT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135798028_135798038delinsCCGAGACTTGT , CM000664.2:g.135798028_135798038delinsCCGAGACTTGT GRCh38
NC_000002.11:g.136555598_136555608delinsCCGAGACTTGT , CM000664.1:g.136555598_136555608delinsCCGAGACTTGT GRCh37
NC_000002.10:g.136272068_136272078delinsCCGAGACTTGT NCBI36
NG_008104.2:g.62132_62142delinsACAAGTCTCGG , LRG_338:g.62132_62142delinsACAAGTCTCGG

Transcript Alleles

HGVS Amino-acid change
ENST00000264162.7:c.4967_4976+1delinsACAAGTCTCGG
ENST00000264162.6:c.4967_4976+1delinsACAAGTCTCGG
ENST00000452974.1:c.3060_3069+1delinsACAAGTCTCGG
NM_002299.2:c.4967_4976+1delinsACAAGTCTCGG , LRG_338t1:c.4967_4976+1delinsACAAGTCTCGG
NM_002299.3:c.4967_4976+1delinsACAAGTCTCGG
XM_017004088.2:c.4967_4976+1delinsACAAGTCTCGG
NM_002299.4:c.4967_4976+1delinsACAAGTCTCGG