Canonical Allele Identifier: CA2698796404

Gene: ALK

Linked Data

• dbSNP Id: rs1325483295

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222421G>T , CM000664.2:g.29222421G>T	GRCh38
NC_000002.11:g.29445287G>T , CM000664.1:g.29445287G>T	GRCh37
NC_000002.10:g.29298791G>T	NCBI36
NG_009445.1:g.704146C>A , LRG_488:g.704146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3451-13C>A MANE Select	ENSP00000373700.3:n.3451-13C>A
ENST00000431873.6:c.678-13C>A
ENST00000638605.1:n.328-13C>A
ENST00000642122.1:c.247-13C>A	ENSP00000493203.1:n.247-13C>A
ENST00000389048.7:c.3451-13C>A	ENSP00000373700.3:n.3451-13C>A
ENST00000431873.5:c.331-13C>A	ENSP00000414027.2:n.331-13C>A
ENST00000453137.1:c.145-13C>A	ENSP00000387488.1:n.145-13C>A
ENST00000618119.4:c.2320-13C>A	ENSP00000482733.1:n.2320-13C>A
NM_004304.4:c.3451-13C>A	NP_004295.2:n.3451-13C>A
NM_001353765.1:c.247-13C>A	NP_001340694.1:n.247-13C>A
XM_024452778.1:c.604-13C>A	XP_024308546.1:n.604-13C>A
XM_024452779.1:c.247-13C>A	XP_024308547.1:n.247-13C>A
NM_004304.5:c.3451-13C>A MANE Select	NP_004295.2:n.3451-13C>A
NM_001353765.2:c.247-13C>A	NP_001340694.1:n.247-13C>A