Canonical Allele Identifier: CA346468077
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs2148178700

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29227059C>A , CM000664.2:g.29227059C>A GRCh38
NC_000002.11:g.29449925C>A , CM000664.1:g.29449925C>A GRCh37
NC_000002.10:g.29303429C>A NCBI36
NG_009445.1:g.699508G>T , LRG_488:g.699508G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.2930G>T MANE Select ENSP00000373700.3:p.Gly977Val
ENST00000431873.6:c.96G>T
ENST00000389048.7:c.2930G>T ENSP00000373700.3:p.Gly977Val
ENST00000618119.4:c.1799G>T ENSP00000482733.1:p.Gly600Val
NM_004304.4:c.2930G>T NP_004295.2:p.Gly977Val
XM_024452778.1:c.83G>T XP_024308546.1:p.Gly28Val
XR_001738688.2:n.3786G>T
NM_004304.5:c.2930G>T MANE Select NP_004295.2:p.Gly977Val