Canonical Allele Identifier: CA346463063

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445237T>A (hg19) ; chr2:g.29222371T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222371T>A , CM000664.2:g.29222371T>A	GRCh38
NC_000002.11:g.29445237T>A , CM000664.1:g.29445237T>A	GRCh37
NC_000002.10:g.29298741T>A	NCBI36
NG_009445.1:g.704196A>T , LRG_488:g.704196A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3488A>T MANE Select	ENSP00000373700.3:p.Asp1163Val
ENST00000431873.6:c.715A>T
ENST00000638605.1:n.365A>T
ENST00000642122.1:c.284A>T	ENSP00000493203.1:p.Asp95Val
ENST00000389048.7:c.3488A>T	ENSP00000373700.3:p.Asp1163Val
ENST00000431873.5:c.368A>T	ENSP00000414027.2:p.Asp123Val
ENST00000453137.1:c.182A>T	ENSP00000387488.1:p.Asp61Val
ENST00000618119.4:c.2357A>T	ENSP00000482733.1:p.Asp786Val
NM_004304.4:c.3488A>T	NP_004295.2:p.Asp1163Val
NM_001353765.1:c.284A>T	NP_001340694.1:p.Asp95Val
XM_024452778.1:c.641A>T	XP_024308546.1:p.Asp214Val
XM_024452779.1:c.284A>T	XP_024308547.1:p.Asp95Val
NM_004304.5:c.3488A>T MANE Select	NP_004295.2:p.Asp1163Val
NM_001353765.2:c.284A>T	NP_001340694.1:p.Asp95Val