Canonical Allele Identifier: CA2749317695

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220882G>C , CM000664.2:g.29220882G>C	GRCh38
NC_000002.11:g.29443748G>C , CM000664.1:g.29443748G>C	GRCh37
NC_000002.10:g.29297252G>C	NCBI36
NG_009445.1:g.705685C>G , LRG_488:g.705685C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3516-47C>G MANE Select	ENSP00000373700.3:n.3516-47C>G
ENST00000431873.6:c.743-47C>G
ENST00000638605.1:n.393-47C>G
ENST00000642122.1:c.312-47C>G	ENSP00000493203.1:n.312-47C>G
ENST00000389048.7:c.3516-47C>G	ENSP00000373700.3:n.3516-47C>G
ENST00000431873.5:c.396-47C>G	ENSP00000414027.2:n.396-47C>G
ENST00000453137.1:c.565C>G	ENSP00000387488.1:n.565C>G
ENST00000618119.4:c.2385-47C>G	ENSP00000482733.1:n.2385-47C>G
NM_004304.4:c.3516-47C>G	NP_004295.2:n.3516-47C>G
NM_001353765.1:c.312-47C>G	NP_001340694.1:n.312-47C>G
XM_024452778.1:c.669-47C>G	XP_024308546.1:n.669-47C>G
XM_024452779.1:c.312-47C>G	XP_024308547.1:n.312-47C>G
NM_004304.5:c.3516-47C>G MANE Select	NP_004295.2:n.3516-47C>G
NM_001353765.2:c.312-47C>G	NP_001340694.1:n.312-47C>G