Canonical Allele Identifier: CA1241325238
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29717524_29717527delinsCTTA , CM000664.2:g.29717524_29717527delinsCTTA GRCh38
NC_000002.11:g.29940390_29940393delinsCTTA , CM000664.1:g.29940390_29940393delinsCTTA GRCh37
NC_000002.10:g.29793894_29793897delinsCTTA NCBI36
NG_009445.1:g.209040_209043delinsTAAG , LRG_488:g.209040_209043delinsTAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.787+51_787+54delinsTAAG MANE Select ENSP00000373700.3:n.787+51_787+54delinsTAAG
ENST00000389048.7:c.787+51_787+54delinsTAAG ENSP00000373700.3:n.787+51_787+54delinsTAAG
ENST00000618119.4:c.-345+51_-345+54delinsTAAG ENSP00000482733.1:n.-345+51_-345+54delinsTAAG
NM_004304.4:c.787+51_787+54delinsTAAG NP_004295.2:n.787+51_787+54delinsTAAG
XR_001738688.2:n.1717+51_1717+54delinsTAAG
NM_004304.5:c.787+51_787+54delinsTAAG MANE Select NP_004295.2:n.787+51_787+54delinsTAAG