Canonical Allele Identifier: CA1241074889

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29197262_29197263delinsGA , CM000664.2:g.29197262_29197263delinsGA GRCh38
NC_000002.11:g.29420128_29420129delinsGA , CM000664.1:g.29420128_29420129delinsGA GRCh37
NC_000002.10:g.29273632_29273633delinsGA NCBI36
NG_009445.1:g.729304_729305delinsTC , LRG_488:g.729304_729305delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000689605.1:c.*256_*257delinsGA (CLIP4) ENSP00000508948.1:n.*256_*257delinsGA
ENST00000389048.8:c.4073+279_4073+280delinsTC (ALK) MANE Select ENSP00000373700.3:n.4073+279_4073+280delinsTC
ENST00000431873.6:c.1300+279_1300+280delinsTC (ALK)
ENST00000638605.1:n.950+279_950+280delinsTC (ALK)
ENST00000642122.1:c.869+279_869+280delinsTC (ALK) ENSP00000493203.1:n.869+279_869+280delinsTC
ENST00000389048.7:c.4073+279_4073+280delinsTC (ALK) ENSP00000373700.3:n.4073+279_4073+280delinsTC
ENST00000431873.5:c.953+279_953+280delinsTC (ALK) ENSP00000414027.2:n.953+279_953+280delinsTC
ENST00000618119.4:c.2942+279_2942+280delinsTC (ALK) ENSP00000482733.1:n.2942+279_2942+280delinsTC
NM_004304.4:c.4073+279_4073+280delinsTC (ALK) NP_004295.2:n.4073+279_4073+280delinsTC
NM_001353765.1:c.869+279_869+280delinsTC (ALK) NP_001340694.1:n.869+279_869+280delinsTC
XM_024452778.1:c.1226+279_1226+280delinsTC (ALK) XP_024308546.1:n.1226+279_1226+280delinsTC
XM_024452779.1:c.869+279_869+280delinsTC (ALK) XP_024308547.1:n.869+279_869+280delinsTC
NM_004304.5:c.4073+279_4073+280delinsTC (ALK) MANE Select NP_004295.2:n.4073+279_4073+280delinsTC
NM_001353765.2:c.869+279_869+280delinsTC (ALK) NP_001340694.1:n.869+279_869+280delinsTC