Canonical Allele Identifier: CA346468431

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29207171C>T , CM000664.2:g.29207171C>T	GRCh38
NC_000002.11:g.29430037C>T , CM000664.1:g.29430037C>T	GRCh37
NC_000002.10:g.29283541C>T	NCBI36
NG_009445.1:g.719396G>A , LRG_488:g.719396G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3938G>A MANE Select	NP_004295.2:p.Trp1313Ter
ENST00000389048.8:c.3938G>A MANE Select	ENSP00000373700.3:p.Trp1313Ter
NM_001353765.1:c.734G>A	NP_001340694.1:p.Trp245Ter
NM_001353765.2:c.734G>A	NP_001340694.1:p.Trp245Ter
NM_004304.4:c.3938G>A	NP_004295.2:p.Trp1313Ter
ENST00000389048.7:c.3938G>A	ENSP00000373700.3:p.Trp1313Ter
ENST00000431873.5:c.818G>A	ENSP00000414027.2:p.Trp273Ter
ENST00000431873.6:c.1165G>A
ENST00000618119.4:c.2807G>A	ENSP00000482733.1:p.Trp936Ter
ENST00000638605.1:n.815G>A
ENST00000642122.1:c.734G>A	ENSP00000493203.1:p.Trp245Ter
XM_024452778.1:c.1091G>A	XP_024308546.1:p.Trp364Ter
XM_024452779.1:c.734G>A	XP_024308547.1:p.Trp245Ter