Canonical Allele Identifier: CA2698983784

Gene: ALK

Linked Data

• dbSNP Id: rs2148166200

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220685C>A , CM000664.2:g.29220685C>A	GRCh38
NC_000002.11:g.29443551C>A , CM000664.1:g.29443551C>A	GRCh37
NC_000002.10:g.29297055C>A	NCBI36
NG_009445.1:g.705882G>T , LRG_488:g.705882G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3645+21G>T MANE Select	ENSP00000373700.3:n.3645+21G>T
ENST00000431873.6:c.872+21G>T
ENST00000638605.1:n.522+21G>T
ENST00000642122.1:c.441+21G>T	ENSP00000493203.1:n.441+21G>T
ENST00000389048.7:c.3645+21G>T	ENSP00000373700.3:n.3645+21G>T
ENST00000431873.5:c.525+21G>T	ENSP00000414027.2:n.525+21G>T
ENST00000618119.4:c.2514+21G>T	ENSP00000482733.1:n.2514+21G>T
NM_004304.4:c.3645+21G>T	NP_004295.2:n.3645+21G>T
NM_001353765.1:c.441+21G>T	NP_001340694.1:n.441+21G>T
XM_024452778.1:c.798+21G>T	XP_024308546.1:n.798+21G>T
XM_024452779.1:c.441+21G>T	XP_024308547.1:n.441+21G>T
NM_004304.5:c.3645+21G>T MANE Select	NP_004295.2:n.3645+21G>T
NM_001353765.2:c.441+21G>T	NP_001340694.1:n.441+21G>T