Canonical Allele Identifier: CA1241090474

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222297_29222298delinsTG , CM000664.2:g.29222297_29222298delinsTG	GRCh38
NC_000002.11:g.29445163_29445164delinsTG , CM000664.1:g.29445163_29445164delinsTG	GRCh37
NC_000002.10:g.29298667_29298668delinsTG	NCBI36
NG_009445.1:g.704269_704270delinsCA , LRG_488:g.704269_704270delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3515+46_3515+47delinsCA MANE Select	ENSP00000373700.3:n.3515+46_3515+47delinsCA
ENST00000431873.6:c.742+46_742+47delinsCA
ENST00000638605.1:n.392+46_392+47delinsCA
ENST00000642122.1:c.311+46_311+47delinsCA	ENSP00000493203.1:n.311+46_311+47delinsCA
ENST00000389048.7:c.3515+46_3515+47delinsCA	ENSP00000373700.3:n.3515+46_3515+47delinsCA
ENST00000431873.5:c.395+46_395+47delinsCA	ENSP00000414027.2:n.395+46_395+47delinsCA
ENST00000453137.1:c.209+46_209+47delinsCA	ENSP00000387488.1:n.209+46_209+47delinsCA
ENST00000618119.4:c.2384+46_2384+47delinsCA	ENSP00000482733.1:n.2384+46_2384+47delinsCA
NM_004304.4:c.3515+46_3515+47delinsCA	NP_004295.2:n.3515+46_3515+47delinsCA
NM_001353765.1:c.311+46_311+47delinsCA	NP_001340694.1:n.311+46_311+47delinsCA
XM_024452778.1:c.668+46_668+47delinsCA	XP_024308546.1:n.668+46_668+47delinsCA
XM_024452779.1:c.311+46_311+47delinsCA	XP_024308547.1:n.311+46_311+47delinsCA
NM_004304.5:c.3515+46_3515+47delinsCA MANE Select	NP_004295.2:n.3515+46_3515+47delinsCA
NM_001353765.2:c.311+46_311+47delinsCA	NP_001340694.1:n.311+46_311+47delinsCA