Canonical Allele Identifier: CA346464122

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222584C>T , CM000664.2:g.29222584C>T	GRCh38
NC_000002.11:g.29445450C>T , CM000664.1:g.29445450C>T	GRCh37
NC_000002.10:g.29298954C>T	NCBI36
NG_009445.1:g.703983G>A , LRG_488:g.703983G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3383G>A MANE Select	NP_004295.2:p.Gly1128Glu
ENST00000389048.8:c.3383G>A MANE Select	ENSP00000373700.3:p.Gly1128Glu
NM_001353765.1:c.179G>A	NP_001340694.1:p.Gly60Glu
NM_001353765.2:c.179G>A	NP_001340694.1:p.Gly60Glu
NM_004304.4:c.3383G>A	NP_004295.2:p.Gly1128Glu
ENST00000389048.7:c.3383G>A	ENSP00000373700.3:p.Gly1128Glu
ENST00000431873.5:c.263G>A	ENSP00000414027.2:p.Gly88Glu
ENST00000431873.6:c.610G>A
ENST00000453137.1:c.77G>A	ENSP00000387488.1:p.Gly26Glu
ENST00000618119.4:c.2252G>A	ENSP00000482733.1:p.Gly751Glu
ENST00000638605.1:n.260G>A
ENST00000642122.1:c.179G>A	ENSP00000493203.1:p.Gly60Glu
XM_024452778.1:c.536G>A	XP_024308546.1:p.Gly179Glu
XM_024452779.1:c.179G>A	XP_024308547.1:p.Gly60Glu