Canonical Allele Identifier: CA346467626

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29449836A>G (hg19) ; chr2:g.29226970A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29226970A>G , CM000664.2:g.29226970A>G	GRCh38
NC_000002.11:g.29449836A>G , CM000664.1:g.29449836A>G	GRCh37
NC_000002.10:g.29303340A>G	NCBI36
NG_009445.1:g.699597T>C , LRG_488:g.699597T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3019T>C MANE Select	ENSP00000373700.3:p.Phe1007Leu
ENST00000431873.6:c.185T>C
ENST00000389048.7:c.3019T>C	ENSP00000373700.3:p.Phe1007Leu
ENST00000618119.4:c.1888T>C	ENSP00000482733.1:p.Phe630Leu
NM_004304.4:c.3019T>C	NP_004295.2:p.Phe1007Leu
XM_024452778.1:c.172T>C	XP_024308546.1:p.Phe58Leu
XR_001738688.2:n.3875T>C
NM_004304.5:c.3019T>C MANE Select	NP_004295.2:p.Phe1007Leu