Canonical Allele Identifier: CA346463034
Gene: ALK HGNC NCBI

Linked Data

dbSNP Id: rs2148168619

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29222367G>C , CM000664.2:g.29222367G>C GRCh38
NC_000002.11:g.29445233G>C , CM000664.1:g.29445233G>C GRCh37
NC_000002.10:g.29298737G>C NCBI36
NG_009445.1:g.704200C>G , LRG_488:g.704200C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389048.8:c.3492C>G MANE Select ENSP00000373700.3:p.Phe1164Leu
ENST00000431873.6:c.719C>G
ENST00000638605.1:n.369C>G
ENST00000642122.1:c.288C>G ENSP00000493203.1:p.Phe96Leu
ENST00000389048.7:c.3492C>G ENSP00000373700.3:p.Phe1164Leu
ENST00000431873.5:c.372C>G ENSP00000414027.2:p.Phe124Leu
ENST00000453137.1:c.186C>G ENSP00000387488.1:p.Phe62Leu
ENST00000618119.4:c.2361C>G ENSP00000482733.1:p.Phe787Leu
NM_004304.4:c.3492C>G NP_004295.2:p.Phe1164Leu
NM_001353765.1:c.288C>G NP_001340694.1:p.Phe96Leu
XM_024452778.1:c.645C>G XP_024308546.1:p.Phe215Leu
XM_024452779.1:c.288C>G XP_024308547.1:p.Phe96Leu
NM_004304.5:c.3492C>G MANE Select NP_004295.2:p.Phe1164Leu
NM_001353765.2:c.288C>G NP_001340694.1:p.Phe96Leu