Canonical Allele Identifier: CA425436034
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs2148178721
MyVariant Identifiers: chr2:g.29449933T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227067T>C , CM000664.2:g.29227067T>C GRCh38
NC_000002.11:g.29449933T>C , CM000664.1:g.29449933T>C GRCh37
NC_000002.10:g.29303437T>C NCBI36
NG_009445.1:g.699500A>G , LRG_488:g.699500A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2922A>G MANE Select ENSP00000373700.3:p.Glu974=
ENST00000431873.6:c.88A>G
ENST00000389048.7:c.2922A>G ENSP00000373700.3:p.Glu974=
ENST00000618119.4:c.1791A>G ENSP00000482733.1:p.Glu597=
NM_004304.4:c.2922A>G NP_004295.2:p.Glu974=
XM_024452778.1:c.75A>G XP_024308546.1:p.Glu25=
XR_001738688.2:n.3778A>G
NM_004304.5:c.2922A>G MANE Select NP_004295.2:p.Glu974=
Search 100 bp 5'
Search 100 bp 3'