Canonical Allele Identifier: CA2658467948
Gene: ALK HGNC NCBI

Linked Data

gnomAD v4: 2-29717487-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29717487G>A , CM000664.2:g.29717487G>A GRCh38
NC_000002.11:g.29940353G>A , CM000664.1:g.29940353G>A GRCh37
NC_000002.10:g.29793857G>A NCBI36
NG_009445.1:g.209080C>T , LRG_488:g.209080C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.787+91C>T MANE Select ENSP00000373700.3:n.787+91C>T
ENST00000389048.7:c.787+91C>T ENSP00000373700.3:n.787+91C>T
ENST00000618119.4:c.-345+91C>T ENSP00000482733.1:n.-345+91C>T
NM_004304.4:c.787+91C>T NP_004295.2:n.787+91C>T
XR_001738688.2:n.1717+91C>T
NM_004304.5:c.787+91C>T MANE Select NP_004295.2:n.787+91C>T