Canonical Allele Identifier: CA346468121
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs2148178719
MyVariant Identifiers: chr2:g.29449932C>G (hg19) chr2:g.29227066C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227066C>G , CM000664.2:g.29227066C>G GRCh38
NC_000002.11:g.29449932C>G , CM000664.1:g.29449932C>G GRCh37
NC_000002.10:g.29303436C>G NCBI36
NG_009445.1:g.699501G>C , LRG_488:g.699501G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2923G>C MANE Select ENSP00000373700.3:p.Gly975Arg
ENST00000431873.6:c.89G>C
ENST00000389048.7:c.2923G>C ENSP00000373700.3:p.Gly975Arg
ENST00000618119.4:c.1792G>C ENSP00000482733.1:p.Gly598Arg
NM_004304.4:c.2923G>C NP_004295.2:p.Gly975Arg
XM_024452778.1:c.76G>C XP_024308546.1:p.Gly26Arg
XR_001738688.2:n.3779G>C
NM_004304.5:c.2923G>C MANE Select NP_004295.2:p.Gly975Arg
Search 100 bp 5'
Search 100 bp 3'