Canonical Allele Identifier: CA346463314

Gene: ALK

Linked Data

• dbSNP Id: rs2148168735
• MyVariant Identifiers: chr2:g.29445268G>A (hg19) ; chr2:g.29222402G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222402G>A , CM000664.2:g.29222402G>A	GRCh38
NC_000002.11:g.29445268G>A , CM000664.1:g.29445268G>A	GRCh37
NC_000002.10:g.29298772G>A	NCBI36
NG_009445.1:g.704165C>T , LRG_488:g.704165C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3457C>T MANE Select	ENSP00000373700.3:p.Pro1153Ser
ENST00000431873.6:c.684C>T
ENST00000638605.1:n.334C>T
ENST00000642122.1:c.253C>T	ENSP00000493203.1:p.Pro85Ser
ENST00000389048.7:c.3457C>T	ENSP00000373700.3:p.Pro1153Ser
ENST00000431873.5:c.337C>T	ENSP00000414027.2:p.Pro113Ser
ENST00000453137.1:c.151C>T	ENSP00000387488.1:p.Pro51Ser
ENST00000618119.4:c.2326C>T	ENSP00000482733.1:p.Pro776Ser
NM_004304.4:c.3457C>T	NP_004295.2:p.Pro1153Ser
NM_001353765.1:c.253C>T	NP_001340694.1:p.Pro85Ser
XM_024452778.1:c.610C>T	XP_024308546.1:p.Pro204Ser
XM_024452779.1:c.253C>T	XP_024308547.1:p.Pro85Ser
NM_004304.5:c.3457C>T MANE Select	NP_004295.2:p.Pro1153Ser
NM_001353765.2:c.253C>T	NP_001340694.1:p.Pro85Ser