Canonical Allele Identifier: CA2658466791
Gene: ALK HGNC NCBI

Linked Data

gnomAD v4: 2-29328624-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328624T>A , CM000664.2:g.29328624T>A GRCh38
NC_000002.11:g.29551490T>A , CM000664.1:g.29551490T>A GRCh37
NC_000002.10:g.29404994T>A NCBI36
NG_009445.1:g.597943A>T , LRG_488:g.597943A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.1283-143A>T MANE Select ENSP00000373700.3:n.1283-143A>T
ENST00000389048.7:c.1283-143A>T ENSP00000373700.3:n.1283-143A>T
ENST00000618119.4:c.152-143A>T ENSP00000482733.1:n.152-143A>T
NM_004304.4:c.1283-143A>T NP_004295.2:n.1283-143A>T
XR_939920.1:n.817+115T>A
XR_939921.1:n.680+6096T>A
XR_001738688.2:n.2213-143A>T
XR_939920.2:n.707+115T>A
XR_939921.2:n.576+6096T>A
NM_004304.5:c.1283-143A>T MANE Select NP_004295.2:n.1283-143A>T