Canonical Allele Identifier: CA346467726

Gene: ALK

Linked Data

• dbSNP Id: rs2148178520
• MyVariant Identifiers: chr2:g.29449869G>T (hg19) ; chr2:g.29227003G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29227003G>T , CM000664.2:g.29227003G>T	GRCh38
NC_000002.11:g.29449869G>T , CM000664.1:g.29449869G>T	GRCh37
NC_000002.10:g.29303373G>T	NCBI36
NG_009445.1:g.699564C>A , LRG_488:g.699564C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.2986C>A MANE Select	ENSP00000373700.3:p.His996Asn
ENST00000431873.6:c.152C>A
ENST00000389048.7:c.2986C>A	ENSP00000373700.3:p.His996Asn
ENST00000618119.4:c.1855C>A	ENSP00000482733.1:p.His619Asn
NM_004304.4:c.2986C>A	NP_004295.2:p.His996Asn
XM_024452778.1:c.139C>A	XP_024308546.1:p.His47Asn
XR_001738688.2:n.3842C>A
NM_004304.5:c.2986C>A MANE Select	NP_004295.2:p.His996Asn