Canonical Allele Identifier: CA346463242

Gene: ALK

Linked Data

• dbSNP Id: rs1057519859
• MyVariant Identifiers: chr2:g.29445258C>A (hg19) ; chr2:g.29222392C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222392C>A , CM000664.2:g.29222392C>A	GRCh38
NC_000002.11:g.29445258C>A , CM000664.1:g.29445258C>A	GRCh37
NC_000002.10:g.29298762C>A	NCBI36
NG_009445.1:g.704175G>T , LRG_488:g.704175G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3467G>T MANE Select	ENSP00000373700.3:p.Cys1156Phe
ENST00000431873.6:c.694G>T
ENST00000638605.1:n.344G>T
ENST00000642122.1:c.263G>T	ENSP00000493203.1:p.Cys88Phe
ENST00000389048.7:c.3467G>T	ENSP00000373700.3:p.Cys1156Phe
ENST00000431873.5:c.347G>T	ENSP00000414027.2:p.Cys116Phe
ENST00000453137.1:c.161G>T	ENSP00000387488.1:p.Cys54Phe
ENST00000618119.4:c.2336G>T	ENSP00000482733.1:p.Cys779Phe
NM_004304.4:c.3467G>T	NP_004295.2:p.Cys1156Phe
NM_001353765.1:c.263G>T	NP_001340694.1:p.Cys88Phe
XM_024452778.1:c.620G>T	XP_024308546.1:p.Cys207Phe
XM_024452779.1:c.263G>T	XP_024308547.1:p.Cys88Phe
NM_004304.5:c.3467G>T MANE Select	NP_004295.2:p.Cys1156Phe
NM_001353765.2:c.263G>T	NP_001340694.1:p.Cys88Phe