Canonical Allele Identifier: CA1241325232
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29717515C= , CM000664.2:g.29717515C= GRCh38
NC_000002.11:g.29940381C= , CM000664.1:g.29940381C= GRCh37
NC_000002.10:g.29793885C= NCBI36
NG_009445.1:g.209052G= , LRG_488:g.209052G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.787+63G= MANE Select ENSP00000373700.3:n.787+63G=
ENST00000389048.7:c.787+63G= ENSP00000373700.3:n.787+63G=
ENST00000618119.4:c.-345+63G= ENSP00000482733.1:n.-345+63G=
NM_004304.4:c.787+63G= NP_004295.2:n.787+63G=
XR_001738688.2:n.1717+63G=
NM_004304.5:c.787+63G= MANE Select NP_004295.2:n.787+63G=