Canonical Allele Identifier: CA346463039

Gene: ALK

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3491T>C MANE Select	ENSP00000373700.3:p.Phe1164Ser
ENST00000431873.6:c.718T>C
ENST00000638605.1:n.368T>C
ENST00000642122.1:c.287T>C	ENSP00000493203.1:p.Phe96Ser
ENST00000389048.7:c.3491T>C	ENSP00000373700.3:p.Phe1164Ser
ENST00000431873.5:c.371T>C	ENSP00000414027.2:p.Phe124Ser
ENST00000453137.1:c.185T>C	ENSP00000387488.1:p.Phe62Ser
ENST00000618119.4:c.2360T>C	ENSP00000482733.1:p.Phe787Ser
NM_004304.4:c.3491T>C	NP_004295.2:p.Phe1164Ser
NM_001353765.1:c.287T>C	NP_001340694.1:p.Phe96Ser
XM_024452778.1:c.644T>C	XP_024308546.1:p.Phe215Ser
XM_024452779.1:c.287T>C	XP_024308547.1:p.Phe96Ser
NM_004304.5:c.3491T>C MANE Select	NP_004295.2:p.Phe1164Ser
NM_001353765.2:c.287T>C	NP_001340694.1:p.Phe96Ser