Canonical Allele Identifier: CA2698999587

Gene: ALK

Linked Data

• dbSNP Id: rs2148168541

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222347_29222348delinsTG , CM000664.2:g.29222347_29222348delinsTG	GRCh38
NC_000002.11:g.29445213_29445214delinsTG , CM000664.1:g.29445213_29445214delinsTG	GRCh37
NC_000002.10:g.29298717_29298718delinsTG	NCBI36
NG_009445.1:g.704219_704220delinsCA , LRG_488:g.704219_704220delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3511_3512delinsCA MANE Select	ENSP00000373700.3:p.Ile1171His
ENST00000431873.6:c.738_739delinsCA
ENST00000638605.1:n.388_389delinsCA
ENST00000642122.1:c.307_308delinsCA	ENSP00000493203.1:p.Ile103His
ENST00000389048.7:c.3511_3512delinsCA	ENSP00000373700.3:p.Ile1171His
ENST00000431873.5:c.391_392delinsCA	ENSP00000414027.2:p.Ile131His
ENST00000453137.1:c.205_206delinsCA	ENSP00000387488.1:p.Ile69His
ENST00000618119.4:c.2380_2381delinsCA	ENSP00000482733.1:p.Ile794His
NM_004304.4:c.3511_3512delinsCA	NP_004295.2:p.Ile1171His
NM_001353765.1:c.307_308delinsCA	NP_001340694.1:p.Ile103His
XM_024452778.1:c.664_665delinsCA	XP_024308546.1:p.Ile222His
XM_024452779.1:c.307_308delinsCA	XP_024308547.1:p.Ile103His
NM_004304.5:c.3511_3512delinsCA MANE Select	NP_004295.2:p.Ile1171His
NM_001353765.2:c.307_308delinsCA	NP_001340694.1:p.Ile103His