Canonical Allele Identifier: CA346472710

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29320871C>T , CM000664.2:g.29320871C>T	GRCh38
NC_000002.11:g.29543737C>T , CM000664.1:g.29543737C>T	GRCh37
NC_000002.10:g.29397241C>T	NCBI36
NG_009445.1:g.605696G>A , LRG_488:g.605696G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.1426G>A MANE Select	NP_004295.2:p.Val476Met
ENST00000389048.8:c.1426G>A MANE Select	ENSP00000373700.3:p.Val476Met
NM_004304.4:c.1426G>A	NP_004295.2:p.Val476Met
ENST00000389048.7:c.1426G>A	ENSP00000373700.3:p.Val476Met
ENST00000618119.4:c.295G>A	ENSP00000482733.1:p.Val99Met
XR_001738688.2:n.2356G>A
XR_244977.3:n.560+898C>T
XR_244977.4:n.459+898C>T
XR_939920.1:n.584-608C>T
XR_939920.2:n.474-608C>T
XR_939921.1:n.572-608C>T
XR_939921.2:n.468-608C>T
XR_939922.1:n.563-608C>T
XR_939922.2:n.462-608C>T
XR_939923.1:n.563-608C>T
XR_939923.3:n.462-608C>T
XR_939924.1:n.563-608C>T
XR_939924.2:n.462-608C>T
XR_939925.1:n.560+898C>T
XR_939925.2:n.459+898C>T
XR_939926.1:n.560+898C>T
XR_939926.2:n.459+898C>T