Canonical Allele Identifier: CA346463783

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222547G>T , CM000664.2:g.29222547G>T	GRCh38
NC_000002.11:g.29445413G>T , CM000664.1:g.29445413G>T	GRCh37
NC_000002.10:g.29298917G>T	NCBI36
NG_009445.1:g.704020C>A , LRG_488:g.704020C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3420C>A MANE Select	NP_004295.2:p.Asn1140Lys
ENST00000389048.8:c.3420C>A MANE Select	ENSP00000373700.3:p.Asn1140Lys
NM_001353765.1:c.216C>A	NP_001340694.1:p.Asn72Lys
NM_001353765.2:c.216C>A	NP_001340694.1:p.Asn72Lys
NM_004304.4:c.3420C>A	NP_004295.2:p.Asn1140Lys
ENST00000389048.7:c.3420C>A	ENSP00000373700.3:p.Asn1140Lys
ENST00000431873.5:c.300C>A	ENSP00000414027.2:p.Asn100Lys
ENST00000431873.6:c.647C>A
ENST00000453137.1:c.114C>A	ENSP00000387488.1:p.Asn38Lys
ENST00000618119.4:c.2289C>A	ENSP00000482733.1:p.Asn763Lys
ENST00000638605.1:n.297C>A
ENST00000642122.1:c.216C>A	ENSP00000493203.1:p.Asn72Lys
XM_024452778.1:c.573C>A	XP_024308546.1:p.Asn191Lys
XM_024452779.1:c.216C>A	XP_024308547.1:p.Asn72Lys