Canonical Allele Identifier: CA346463043

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29445234A>C (hg19) ; chr2:g.29222368A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222368A>C , CM000664.2:g.29222368A>C	GRCh38
NC_000002.11:g.29445234A>C , CM000664.1:g.29445234A>C	GRCh37
NC_000002.10:g.29298738A>C	NCBI36
NG_009445.1:g.704199T>G , LRG_488:g.704199T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3491T>G MANE Select	ENSP00000373700.3:p.Phe1164Cys
ENST00000431873.6:c.718T>G
ENST00000638605.1:n.368T>G
ENST00000642122.1:c.287T>G	ENSP00000493203.1:p.Phe96Cys
ENST00000389048.7:c.3491T>G	ENSP00000373700.3:p.Phe1164Cys
ENST00000431873.5:c.371T>G	ENSP00000414027.2:p.Phe124Cys
ENST00000453137.1:c.185T>G	ENSP00000387488.1:p.Phe62Cys
ENST00000618119.4:c.2360T>G	ENSP00000482733.1:p.Phe787Cys
NM_004304.4:c.3491T>G	NP_004295.2:p.Phe1164Cys
NM_001353765.1:c.287T>G	NP_001340694.1:p.Phe96Cys
XM_024452778.1:c.644T>G	XP_024308546.1:p.Phe215Cys
XM_024452779.1:c.287T>G	XP_024308547.1:p.Phe96Cys
NM_004304.5:c.3491T>G MANE Select	NP_004295.2:p.Phe1164Cys
NM_001353765.2:c.287T>G	NP_001340694.1:p.Phe96Cys