Canonical Allele Identifier: CA2658458455

Gene: ALK

Linked Data

• gnomAD v4: 2-29222497-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222497A>C , CM000664.2:g.29222497A>C	GRCh38
NC_000002.11:g.29445363A>C , CM000664.1:g.29445363A>C	GRCh37
NC_000002.10:g.29298867A>C	NCBI36
NG_009445.1:g.704070T>G , LRG_488:g.704070T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3450+20T>G MANE Select	ENSP00000373700.3:n.3450+20T>G
ENST00000431873.6:c.677+20T>G
ENST00000638605.1:n.327+20T>G
ENST00000642122.1:c.246+20T>G	ENSP00000493203.1:n.246+20T>G
ENST00000389048.7:c.3450+20T>G	ENSP00000373700.3:n.3450+20T>G
ENST00000431873.5:c.330+20T>G	ENSP00000414027.2:n.330+20T>G
ENST00000453137.1:c.144+20T>G	ENSP00000387488.1:n.144+20T>G
ENST00000618119.4:c.2319+20T>G	ENSP00000482733.1:n.2319+20T>G
NM_004304.4:c.3450+20T>G	NP_004295.2:n.3450+20T>G
NM_001353765.1:c.246+20T>G	NP_001340694.1:n.246+20T>G
XM_024452778.1:c.603+20T>G	XP_024308546.1:n.603+20T>G
XM_024452779.1:c.246+20T>G	XP_024308547.1:n.246+20T>G
NM_004304.5:c.3450+20T>G MANE Select	NP_004295.2:n.3450+20T>G
NM_001353765.2:c.246+20T>G	NP_001340694.1:n.246+20T>G