Canonical Allele Identifier: CA346472648
Community Standard Title: NM_004304.5(ALK):c.1441A>T (p.Asn481Tyr)
Gene: ALK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29320856T>A , CM000664.2:g.29320856T>A GRCh38
NC_000002.11:g.29543722T>A , CM000664.1:g.29543722T>A GRCh37
NC_000002.10:g.29397226T>A NCBI36
NG_009445.1:g.605711A>T , LRG_488:g.605711A>T

Transcript Alleles

HGVS Amino-acid Change
NM_004304.5:c.1441A>T MANE Select NP_004295.2:p.Asn481Tyr
ENST00000389048.8:c.1441A>T MANE Select ENSP00000373700.3:p.Asn481Tyr
NM_004304.4:c.1441A>T NP_004295.2:p.Asn481Tyr
ENST00000389048.7:c.1441A>T ENSP00000373700.3:p.Asn481Tyr
ENST00000618119.4:c.310A>T ENSP00000482733.1:p.Asn104Tyr
XR_001738688.2:n.2371A>T
XR_244977.3:n.560+883T>A
XR_244977.4:n.459+883T>A
XR_939920.1:n.584-623T>A
XR_939920.2:n.474-623T>A
XR_939921.1:n.572-623T>A
XR_939921.2:n.468-623T>A
XR_939922.1:n.563-623T>A
XR_939922.2:n.462-623T>A
XR_939923.1:n.563-623T>A
XR_939923.3:n.462-623T>A
XR_939924.1:n.563-623T>A
XR_939924.2:n.462-623T>A
XR_939925.1:n.560+883T>A
XR_939925.2:n.459+883T>A
XR_939926.1:n.560+883T>A
XR_939926.2:n.459+883T>A