Canonical Allele Identifier: CA1241090524

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222383T= , CM000664.2:g.29222383T=	GRCh38
NC_000002.11:g.29445249T= , CM000664.1:g.29445249T=	GRCh37
NC_000002.10:g.29298753T=	NCBI36
NG_009445.1:g.704184A= , LRG_488:g.704184A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3476A= MANE Select	ENSP00000373700.3:p.Gln1159=
ENST00000431873.6:c.703A=
ENST00000638605.1:n.353A=
ENST00000642122.1:c.272A=	ENSP00000493203.1:p.Gln91=
ENST00000389048.7:c.3476A=	ENSP00000373700.3:p.Gln1159=
ENST00000431873.5:c.356A=	ENSP00000414027.2:p.Gln119=
ENST00000453137.1:c.170A=	ENSP00000387488.1:p.Gln57=
ENST00000618119.4:c.2345A=	ENSP00000482733.1:p.Gln782=
NM_004304.4:c.3476A=	NP_004295.2:p.Gln1159=
NM_001353765.1:c.272A=	NP_001340694.1:p.Gln91=
XM_024452778.1:c.629A=	XP_024308546.1:p.Gln210=
XM_024452779.1:c.272A=	XP_024308547.1:p.Gln91=
NM_004304.5:c.3476A= MANE Select	NP_004295.2:p.Gln1159=
NM_001353765.2:c.272A=	NP_001340694.1:p.Gln91=