Canonical Allele Identifier: CA2573134527

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29214094A>G , CM000664.2:g.29214094A>G	GRCh38
NC_000002.11:g.29436960A>G , CM000664.1:g.29436960A>G	GRCh37
NC_000002.10:g.29290464A>G	NCBI36
NG_009445.1:g.712473T>C , LRG_488:g.712473T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.3646-13T>C MANE Select	NP_004295.2:n.3646-13T>C
ENST00000389048.8:c.3646-13T>C MANE Select	ENSP00000373700.3:n.3646-13T>C
NM_001353765.1:c.442-13T>C	NP_001340694.1:n.442-13T>C
NM_001353765.2:c.442-13T>C	NP_001340694.1:n.442-13T>C
NM_004304.4:c.3646-13T>C	NP_004295.2:n.3646-13T>C
ENST00000389048.7:c.3646-13T>C	ENSP00000373700.3:n.3646-13T>C
ENST00000431873.5:c.526-13T>C	ENSP00000414027.2:n.526-13T>C
ENST00000431873.6:c.873-13T>C
ENST00000618119.4:c.2515-13T>C	ENSP00000482733.1:n.2515-13T>C
ENST00000638605.1:n.523-13T>C
ENST00000642122.1:c.442-13T>C	ENSP00000493203.1:n.442-13T>C
XM_024452778.1:c.799-13T>C	XP_024308546.1:n.799-13T>C
XM_024452779.1:c.442-13T>C	XP_024308547.1:n.442-13T>C