Canonical Allele Identifier: CA346464574

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29223341C>A , CM000664.2:g.29223341C>A	GRCh38
NC_000002.11:g.29446207C>A , CM000664.1:g.29446207C>A	GRCh37
NC_000002.10:g.29299711C>A	NCBI36
NG_009445.1:g.703226G>T , LRG_488:g.703226G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3359+1G>T MANE Select	NP_004295.2:n.3359+1G>T
ENST00000389048.8:c.3359+1G>T MANE Select	ENSP00000373700.3:n.3359+1G>T
NM_001353765.1:c.155+1G>T	NP_001340694.1:n.155+1G>T
NM_001353765.2:c.155+1G>T	NP_001340694.1:n.155+1G>T
NM_004304.4:c.3359+1G>T	NP_004295.2:n.3359+1G>T
ENST00000389048.7:c.3359+1G>T	ENSP00000373700.3:n.3359+1G>T
ENST00000431873.5:c.239+1G>T	ENSP00000414027.2:n.239+1G>T
ENST00000431873.6:c.586+1G>T
ENST00000453137.1:c.53+1G>T	ENSP00000387488.1:n.53+1G>T
ENST00000618119.4:c.2228+1G>T	ENSP00000482733.1:n.2228+1G>T
ENST00000638605.1:n.236+1G>T
ENST00000642122.1:c.155+1G>T	ENSP00000493203.1:n.155+1G>T
XM_024452778.1:c.512+1G>T	XP_024308546.1:n.512+1G>T
XM_024452779.1:c.155+1G>T	XP_024308547.1:n.155+1G>T