Canonical Allele Identifier: CA2541481654

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67490287_67490288insGG , CM000673.2:g.67490287_67490288insGG GRCh38
NC_000011.9:g.67257758_67257759insGG , CM000673.1:g.67257758_67257759insGG GRCh37
NC_000011.8:g.67014334_67014335insGG NCBI36
NG_008969.1:g.12254_12255insGG , LRG_460:g.12254_12255insGG

Transcript Alleles

HGVS Amino-acid change
ENST00000525341.2:c.623-29_623-28insGG (AIP)
ENST00000528641.7:c.457-29_457-28insGG (AIP) ENSP00000434982.3:n.457-29_457-28insGG
ENST00000529797.2:n.1158-29_1158-28insGG (AIP)
ENST00000682324.1:c.469-710_469-709insGG (AIP) ENSP00000508017.1:n.469-710_469-709insGG
ENST00000682659.1:c.277-29_277-28insGG (AIP) ENSP00000507351.1:n.277-29_277-28insGG
ENST00000682699.1:c.646-29_646-28insGG (AIP) ENSP00000507935.1:n.646-29_646-28insGG
ENST00000683237.1:c.646-29_646-28insGG (AIP) ENSP00000507343.1:n.646-29_646-28insGG
ENST00000683856.1:c.469-29_469-28insGG (AIP) ENSP00000507979.1:n.469-29_469-28insGG
ENST00000684006.1:c.646-29_646-28insGG (AIP) ENSP00000507269.1:n.646-29_646-28insGG
ENST00000684657.1:c.466-29_466-28insGG (AIP) ENSP00000507961.1:n.466-29_466-28insGG
ENST00000279146.8:c.646-29_646-28insGG (AIP) MANE Select ENSP00000279146.3:n.646-29_646-28insGG
ENST00000279146.7:c.646-29_646-28insGG (AIP) ENSP00000279146.3:n.646-29_646-28insGG
ENST00000525341.1:c.298-29_298-28insGG (AIP) ENSP00000476993.1:n.298-29_298-28insGG
ENST00000528641.6:c.457-29_457-28insGG (AIP) ENSP00000434982.2:n.457-29_457-28insGG
NM_001302959.1:c.469-29_469-28insGG (AIP) NP_001289888.1:n.469-29_469-28insGG
NM_001302960.1:c.646-29_646-28insGG (AIP) NP_001289889.1:n.646-29_646-28insGG
NM_003977.3:c.646-29_646-28insGG (AIP) NP_003968.3:n.646-29_646-28insGG
NR_106810.1:n.43_44insGG (MIR6752)
XM_024448761.1:c.646-29_646-28insGG (AIP) XP_024304529.1:n.646-29_646-28insGG
NM_003977.4:c.646-29_646-28insGG (AIP) MANE Select NP_003968.3:n.646-29_646-28insGG
NM_001302960.2:c.646-29_646-28insGG (AIP) NP_001289889.1:n.646-29_646-28insGG
NM_001302959.2:c.469-29_469-28insGG (AIP) NP_001289888.1:n.469-29_469-28insGG