Canonical Allele Identifier: CA2658466672
Gene: ALK HGNC NCBI

Linked Data

gnomAD v4: 2-29328508-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328508T>C , CM000664.2:g.29328508T>C GRCh38
NC_000002.11:g.29551374T>C , CM000664.1:g.29551374T>C GRCh37
NC_000002.10:g.29404878T>C NCBI36
NG_009445.1:g.598059A>G , LRG_488:g.598059A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1283-27A>G MANE Select ENSP00000373700.3:n.1283-27A>G
ENST00000389048.7:c.1283-27A>G ENSP00000373700.3:n.1283-27A>G
ENST00000618119.4:c.152-27A>G ENSP00000482733.1:n.152-27A>G
NM_004304.4:c.1283-27A>G NP_004295.2:n.1283-27A>G
XR_939920.1:n.816T>C
XR_939921.1:n.680+5980T>C
XR_001738688.2:n.2213-27A>G
XR_939920.2:n.706T>C
XR_939921.2:n.576+5980T>C
NM_004304.5:c.1283-27A>G MANE Select NP_004295.2:n.1283-27A>G
Search 100 bp 5'
Search 100 bp 3'