Canonical Allele Identifier: CA346474248
Gene: ALK HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.29551266C>G (hg19) chr2:g.29328400C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29328400C>G , CM000664.2:g.29328400C>G GRCh38
NC_000002.11:g.29551266C>G , CM000664.1:g.29551266C>G GRCh37
NC_000002.10:g.29404770C>G NCBI36
NG_009445.1:g.598167G>C , LRG_488:g.598167G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000389048.8:c.1364G>C MANE Select ENSP00000373700.3:p.Cys455Ser
ENST00000389048.7:c.1364G>C ENSP00000373700.3:p.Cys455Ser
ENST00000618119.4:c.233G>C ENSP00000482733.1:p.Cys78Ser
NM_004304.4:c.1364G>C NP_004295.2:p.Cys455Ser
XR_939920.1:n.708C>G
XR_939921.1:n.680+5872C>G
XR_001738688.2:n.2294G>C
XR_939920.2:n.598C>G
XR_939921.2:n.576+5872C>G
NM_004304.5:c.1364G>C MANE Select NP_004295.2:p.Cys455Ser
Search 100 bp 5'
Search 100 bp 3'