Canonical Allele Identifier: CA2698823587

Gene: ALK

Linked Data

• dbSNP Id: rs1669783358

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220854T>A , CM000664.2:g.29220854T>A	GRCh38
NC_000002.11:g.29443720T>A , CM000664.1:g.29443720T>A	GRCh37
NC_000002.10:g.29297224T>A	NCBI36
NG_009445.1:g.705713A>T , LRG_488:g.705713A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3516-19A>T MANE Select	ENSP00000373700.3:n.3516-19A>T
ENST00000431873.6:c.743-19A>T
ENST00000638605.1:n.393-19A>T
ENST00000642122.1:c.312-19A>T	ENSP00000493203.1:n.312-19A>T
ENST00000389048.7:c.3516-19A>T	ENSP00000373700.3:n.3516-19A>T
ENST00000431873.5:c.396-19A>T	ENSP00000414027.2:n.396-19A>T
ENST00000618119.4:c.2385-19A>T	ENSP00000482733.1:n.2385-19A>T
NM_004304.4:c.3516-19A>T	NP_004295.2:n.3516-19A>T
NM_001353765.1:c.312-19A>T	NP_001340694.1:n.312-19A>T
XM_024452778.1:c.669-19A>T	XP_024308546.1:n.669-19A>T
XM_024452779.1:c.312-19A>T	XP_024308547.1:n.312-19A>T
NM_004304.5:c.3516-19A>T MANE Select	NP_004295.2:n.3516-19A>T
NM_001353765.2:c.312-19A>T	NP_001340694.1:n.312-19A>T