Canonical Allele Identifier: CA1593933
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs779030556
gnomAD v2: 2-29445296-G-A
gnomAD v4: 2-29222430-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29222430G>A , CM000664.2:g.29222430G>A GRCh38
NC_000002.11:g.29445296G>A , CM000664.1:g.29445296G>A GRCh37
NC_000002.10:g.29298800G>A NCBI36
NG_009445.1:g.704137C>T , LRG_488:g.704137C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3451-22C>T MANE Select ENSP00000373700.3:n.3451-22C>T
ENST00000431873.6:c.678-22C>T
ENST00000638605.1:n.328-22C>T
ENST00000642122.1:c.247-22C>T ENSP00000493203.1:n.247-22C>T
ENST00000389048.7:c.3451-22C>T ENSP00000373700.3:n.3451-22C>T
ENST00000431873.5:c.331-22C>T ENSP00000414027.2:n.331-22C>T
ENST00000453137.1:c.145-22C>T ENSP00000387488.1:n.145-22C>T
ENST00000618119.4:c.2320-22C>T ENSP00000482733.1:n.2320-22C>T
NM_004304.4:c.3451-22C>T NP_004295.2:n.3451-22C>T
NM_001353765.1:c.247-22C>T NP_001340694.1:n.247-22C>T
XM_024452778.1:c.604-22C>T XP_024308546.1:n.604-22C>T
XM_024452779.1:c.247-22C>T XP_024308547.1:n.247-22C>T
NM_004304.5:c.3451-22C>T MANE Select NP_004295.2:n.3451-22C>T
NM_001353765.2:c.247-22C>T NP_001340694.1:n.247-22C>T