Canonical Allele Identifier: CA425619442

Gene: ALK

Linked Data

• dbSNP Id: rs2148166662
• MyVariant Identifiers: chr2:g.29443680A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220814A>T , CM000664.2:g.29220814A>T	GRCh38
NC_000002.11:g.29443680A>T , CM000664.1:g.29443680A>T	GRCh37
NC_000002.10:g.29297184A>T	NCBI36
NG_009445.1:g.705753T>A , LRG_488:g.705753T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3537T>A MANE Select	ENSP00000373700.3:p.Ile1179=
ENST00000431873.6:c.764T>A
ENST00000638605.1:n.414T>A
ENST00000642122.1:c.333T>A	ENSP00000493203.1:p.Ile111=
ENST00000389048.7:c.3537T>A	ENSP00000373700.3:p.Ile1179=
ENST00000431873.5:c.417T>A	ENSP00000414027.2:p.Ile139=
ENST00000618119.4:c.2406T>A	ENSP00000482733.1:p.Ile802=
NM_004304.4:c.3537T>A	NP_004295.2:p.Ile1179=
NM_001353765.1:c.333T>A	NP_001340694.1:p.Ile111=
XM_024452778.1:c.690T>A	XP_024308546.1:p.Ile230=
XM_024452779.1:c.333T>A	XP_024308547.1:p.Ile111=
NM_004304.5:c.3537T>A MANE Select	NP_004295.2:p.Ile1179=
NM_001353765.2:c.333T>A	NP_001340694.1:p.Ile111=