Canonical Allele Identifier: CA425619450

Gene: ALK

Linked Data

• MyVariant Identifiers: chr2:g.29443743A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220877A>G , CM000664.2:g.29220877A>G	GRCh38
NC_000002.11:g.29443743A>G , CM000664.1:g.29443743A>G	GRCh37
NC_000002.10:g.29297247A>G	NCBI36
NG_009445.1:g.705690T>C , LRG_488:g.705690T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3516-42T>C MANE Select	ENSP00000373700.3:n.3516-42T>C
ENST00000431873.6:c.743-42T>C
ENST00000638605.1:n.393-42T>C
ENST00000642122.1:c.312-42T>C	ENSP00000493203.1:n.312-42T>C
ENST00000389048.7:c.3516-42T>C	ENSP00000373700.3:n.3516-42T>C
ENST00000431873.5:c.396-42T>C	ENSP00000414027.2:n.396-42T>C
ENST00000453137.1:c.570T>C	ENSP00000387488.1:n.570T>C
ENST00000618119.4:c.2385-42T>C	ENSP00000482733.1:n.2385-42T>C
NM_004304.4:c.3516-42T>C	NP_004295.2:n.3516-42T>C
NM_001353765.1:c.312-42T>C	NP_001340694.1:n.312-42T>C
XM_024452778.1:c.669-42T>C	XP_024308546.1:n.669-42T>C
XM_024452779.1:c.312-42T>C	XP_024308547.1:n.312-42T>C
NM_004304.5:c.3516-42T>C MANE Select	NP_004295.2:n.3516-42T>C
NM_001353765.2:c.312-42T>C	NP_001340694.1:n.312-42T>C