Canonical Allele Identifier: CA767512184

Gene: ALK

Linked Data

• dbSNP Id: rs1263810152
• gnomAD v3: 2-29220867-A-T
• gnomAD v4: 2-29220867-A-T
• MyVariant Identifiers: chr2:g.29443733A>T (hg19) ; chr2:g.29220867A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220867A>T , CM000664.2:g.29220867A>T	GRCh38
NC_000002.11:g.29443733A>T , CM000664.1:g.29443733A>T	GRCh37
NC_000002.10:g.29297237A>T	NCBI36
NG_009445.1:g.705700T>A , LRG_488:g.705700T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3516-32T>A MANE Select	ENSP00000373700.3:n.3516-32T>A
ENST00000431873.6:c.743-32T>A
ENST00000638605.1:n.393-32T>A
ENST00000642122.1:c.312-32T>A	ENSP00000493203.1:n.312-32T>A
ENST00000389048.7:c.3516-32T>A	ENSP00000373700.3:n.3516-32T>A
ENST00000431873.5:c.396-32T>A	ENSP00000414027.2:n.396-32T>A
ENST00000618119.4:c.2385-32T>A	ENSP00000482733.1:n.2385-32T>A
NM_004304.4:c.3516-32T>A	NP_004295.2:n.3516-32T>A
NM_001353765.1:c.312-32T>A	NP_001340694.1:n.312-32T>A
XM_024452778.1:c.669-32T>A	XP_024308546.1:n.669-32T>A
XM_024452779.1:c.312-32T>A	XP_024308547.1:n.312-32T>A
NM_004304.5:c.3516-32T>A MANE Select	NP_004295.2:n.3516-32T>A
NM_001353765.2:c.312-32T>A	NP_001340694.1:n.312-32T>A