Canonical Allele Identifier: CA1241090586
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29222491_29222492delinsAG , CM000664.2:g.29222491_29222492delinsAG GRCh38
NC_000002.11:g.29445357_29445358delinsAG , CM000664.1:g.29445357_29445358delinsAG GRCh37
NC_000002.10:g.29298861_29298862delinsAG NCBI36
NG_009445.1:g.704075_704076delinsCT , LRG_488:g.704075_704076delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.3450+25_3450+26delinsCT MANE Select ENSP00000373700.3:n.3450+25_3450+26delins...
ENST00000431873.6:c.677+25_677+26delinsCT
ENST00000638605.1:n.327+25_327+26delinsCT
ENST00000642122.1:c.246+25_246+26delinsCT ENSP00000493203.1:n.246+25_246+26delinsCT...
ENST00000389048.7:c.3450+25_3450+26delinsCT ENSP00000373700.3:n.3450+25_3450+26delins...
ENST00000431873.5:c.330+25_330+26delinsCT ENSP00000414027.2:n.330+25_330+26delinsCT...
ENST00000453137.1:c.144+25_144+26delinsCT ENSP00000387488.1:n.144+25_144+26delinsCT...
ENST00000618119.4:c.2319+25_2319+26delinsCT ENSP00000482733.1:n.2319+25_2319+26delins...
NM_004304.4:c.3450+25_3450+26delinsCT NP_004295.2:n.3450+25_3450+26delinsCT
NM_001353765.1:c.246+25_246+26delinsCT NP_001340694.1:n.246+25_246+26delinsCT
XM_024452778.1:c.603+25_603+26delinsCT XP_024308546.1:n.603+25_603+26delinsCT
XM_024452779.1:c.246+25_246+26delinsCT XP_024308547.1:n.246+25_246+26delinsCT
NM_004304.5:c.3450+25_3450+26delinsCT MANE Select NP_004295.2:n.3450+25_3450+26delinsCT
NM_001353765.2:c.246+25_246+26delinsCT NP_001340694.1:n.246+25_246+26delinsCT