Canonical Allele Identifier: CA346463163

Gene: ALK

Linked Data

• dbSNP Id: rs2148168660
• MyVariant Identifiers: chr2:g.29445247C>A (hg19) ; chr2:g.29222381C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222381C>A , CM000664.2:g.29222381C>A	GRCh38
NC_000002.11:g.29445247C>A , CM000664.1:g.29445247C>A	GRCh37
NC_000002.10:g.29298751C>A	NCBI36
NG_009445.1:g.704186G>T , LRG_488:g.704186G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3478G>T MANE Select	ENSP00000373700.3:p.Asp1160Tyr
ENST00000431873.6:c.705G>T
ENST00000638605.1:n.355G>T
ENST00000642122.1:c.274G>T	ENSP00000493203.1:p.Asp92Tyr
ENST00000389048.7:c.3478G>T	ENSP00000373700.3:p.Asp1160Tyr
ENST00000431873.5:c.358G>T	ENSP00000414027.2:p.Asp120Tyr
ENST00000453137.1:c.172G>T	ENSP00000387488.1:p.Asp58Tyr
ENST00000618119.4:c.2347G>T	ENSP00000482733.1:p.Asp783Tyr
NM_004304.4:c.3478G>T	NP_004295.2:p.Asp1160Tyr
NM_001353765.1:c.274G>T	NP_001340694.1:p.Asp92Tyr
XM_024452778.1:c.631G>T	XP_024308546.1:p.Asp211Tyr
XM_024452779.1:c.274G>T	XP_024308547.1:p.Asp92Tyr
NM_004304.5:c.3478G>T MANE Select	NP_004295.2:p.Asp1160Tyr
NM_001353765.2:c.274G>T	NP_001340694.1:p.Asp92Tyr