Canonical Allele Identifier: CA1593788

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29209883G>A , CM000664.2:g.29209883G>A	GRCh38
NC_000002.11:g.29432749G>A , CM000664.1:g.29432749G>A	GRCh37
NC_000002.10:g.29286253G>A	NCBI36
NG_009445.1:g.716684C>T , LRG_488:g.716684C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3744-5C>T MANE Select	NP_004295.2:n.3744-5C>T
ENST00000389048.8:c.3744-5C>T MANE Select	ENSP00000373700.3:n.3744-5C>T
NM_001353765.1:c.540-5C>T	NP_001340694.1:n.540-5C>T
NM_001353765.2:c.540-5C>T	NP_001340694.1:n.540-5C>T
NM_004304.4:c.3744-5C>T	NP_004295.2:n.3744-5C>T
ENST00000389048.7:c.3744-5C>T	ENSP00000373700.3:n.3744-5C>T
ENST00000431873.5:c.624-5C>T	ENSP00000414027.2:n.624-5C>T
ENST00000431873.6:c.971-5C>T
ENST00000618119.4:c.2613-5C>T	ENSP00000482733.1:n.2613-5C>T
ENST00000638605.1:n.621-5C>T
ENST00000642122.1:c.540-5C>T	ENSP00000493203.1:n.540-5C>T
XM_024452778.1:c.897-5C>T	XP_024308546.1:n.897-5C>T
XM_024452779.1:c.540-5C>T	XP_024308547.1:n.540-5C>T