Canonical Allele Identifier: CA2658467958
Gene: ALK HGNC NCBI

Linked Data

gnomAD v4: 2-29717508-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29717508T>A , CM000664.2:g.29717508T>A GRCh38
NC_000002.11:g.29940374T>A , CM000664.1:g.29940374T>A GRCh37
NC_000002.10:g.29793878T>A NCBI36
NG_009445.1:g.209059A>T , LRG_488:g.209059A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.787+70A>T MANE Select ENSP00000373700.3:n.787+70A>T
ENST00000389048.7:c.787+70A>T ENSP00000373700.3:n.787+70A>T
ENST00000618119.4:c.-345+70A>T ENSP00000482733.1:n.-345+70A>T
NM_004304.4:c.787+70A>T NP_004295.2:n.787+70A>T
XR_001738688.2:n.1717+70A>T
NM_004304.5:c.787+70A>T MANE Select NP_004295.2:n.787+70A>T
Search 100 bp 5'
Search 100 bp 3'