Canonical Allele Identifier: CA346473087

Gene: ALK

Linked Data

• dbSNP Id: rs2148166559
• MyVariant Identifiers: chr2:g.29443646G>C (hg19) ; chr2:g.29220780G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220780G>C , CM000664.2:g.29220780G>C	GRCh38
NC_000002.11:g.29443646G>C , CM000664.1:g.29443646G>C	GRCh37
NC_000002.10:g.29297150G>C	NCBI36
NG_009445.1:g.705787C>G , LRG_488:g.705787C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3571C>G MANE Select	ENSP00000373700.3:p.Pro1191Ala
ENST00000431873.6:c.798C>G
ENST00000638605.1:n.448C>G
ENST00000642122.1:c.367C>G	ENSP00000493203.1:p.Pro123Ala
ENST00000389048.7:c.3571C>G	ENSP00000373700.3:p.Pro1191Ala
ENST00000431873.5:c.451C>G	ENSP00000414027.2:p.Pro151Ala
ENST00000618119.4:c.2440C>G	ENSP00000482733.1:p.Pro814Ala
NM_004304.4:c.3571C>G	NP_004295.2:p.Pro1191Ala
NM_001353765.1:c.367C>G	NP_001340694.1:p.Pro123Ala
XM_024452778.1:c.724C>G	XP_024308546.1:p.Pro242Ala
XM_024452779.1:c.367C>G	XP_024308547.1:p.Pro123Ala
NM_004304.5:c.3571C>G MANE Select	NP_004295.2:p.Pro1191Ala
NM_001353765.2:c.367C>G	NP_001340694.1:p.Pro123Ala