Canonical Allele Identifier: CA2698983807

Gene: ALK

Linked Data

• dbSNP Id: rs2148166204

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220687A>T , CM000664.2:g.29220687A>T	GRCh38
NC_000002.11:g.29443553A>T , CM000664.1:g.29443553A>T	GRCh37
NC_000002.10:g.29297057A>T	NCBI36
NG_009445.1:g.705880T>A , LRG_488:g.705880T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3645+19T>A MANE Select	ENSP00000373700.3:n.3645+19T>A
ENST00000431873.6:c.872+19T>A
ENST00000638605.1:n.522+19T>A
ENST00000642122.1:c.441+19T>A	ENSP00000493203.1:n.441+19T>A
ENST00000389048.7:c.3645+19T>A	ENSP00000373700.3:n.3645+19T>A
ENST00000431873.5:c.525+19T>A	ENSP00000414027.2:n.525+19T>A
ENST00000618119.4:c.2514+19T>A	ENSP00000482733.1:n.2514+19T>A
NM_004304.4:c.3645+19T>A	NP_004295.2:n.3645+19T>A
NM_001353765.1:c.441+19T>A	NP_001340694.1:n.441+19T>A
XM_024452778.1:c.798+19T>A	XP_024308546.1:n.798+19T>A
XM_024452779.1:c.441+19T>A	XP_024308547.1:n.441+19T>A
NM_004304.5:c.3645+19T>A MANE Select	NP_004295.2:n.3645+19T>A
NM_001353765.2:c.441+19T>A	NP_001340694.1:n.441+19T>A