Canonical Allele Identifier: CA346463055

Gene: ALK

Linked Data

• dbSNP Id: rs2148168620
• MyVariant Identifiers: chr2:g.29445235A>T (hg19) ; chr2:g.29222369A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222369A>T , CM000664.2:g.29222369A>T	GRCh38
NC_000002.11:g.29445235A>T , CM000664.1:g.29445235A>T	GRCh37
NC_000002.10:g.29298739A>T	NCBI36
NG_009445.1:g.704198T>A , LRG_488:g.704198T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3490T>A MANE Select	ENSP00000373700.3:p.Phe1164Ile
ENST00000431873.6:c.717T>A
ENST00000638605.1:n.367T>A
ENST00000642122.1:c.286T>A	ENSP00000493203.1:p.Phe96Ile
ENST00000389048.7:c.3490T>A	ENSP00000373700.3:p.Phe1164Ile
ENST00000431873.5:c.370T>A	ENSP00000414027.2:p.Phe124Ile
ENST00000453137.1:c.184T>A	ENSP00000387488.1:p.Phe62Ile
ENST00000618119.4:c.2359T>A	ENSP00000482733.1:p.Phe787Ile
NM_004304.4:c.3490T>A	NP_004295.2:p.Phe1164Ile
NM_001353765.1:c.286T>A	NP_001340694.1:p.Phe96Ile
XM_024452778.1:c.643T>A	XP_024308546.1:p.Phe215Ile
XM_024452779.1:c.286T>A	XP_024308547.1:p.Phe96Ile
NM_004304.5:c.3490T>A MANE Select	NP_004295.2:p.Phe1164Ile
NM_001353765.2:c.286T>A	NP_001340694.1:p.Phe96Ile