Canonical Allele Identifier: CA2576925231

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220820_29220834del , CM000664.2:g.29220820_29220834del	GRCh38
NC_000002.11:g.29443686_29443700del , CM000664.1:g.29443686_29443700del	GRCh37
NC_000002.10:g.29297190_29297204del	NCBI36
NG_009445.1:g.705735_705749del , LRG_488:g.705735_705749del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3519_3533del MANE Select	ENSP00000373700.3:p.Lys1173_Gln1177del
ENST00000431873.6:c.746_760del
ENST00000638605.1:n.396_410del
ENST00000642122.1:c.315_329del	ENSP00000493203.1:p.Lys105_Gln109del
ENST00000389048.7:c.3519_3533del	ENSP00000373700.3:p.Lys1173_Gln1177del
ENST00000431873.5:c.399_413del	ENSP00000414027.2:p.Lys133_Gln137del
ENST00000618119.4:c.2388_2402del	ENSP00000482733.1:p.Lys796_Gln800del
NM_004304.4:c.3519_3533del	NP_004295.2:p.Lys1173_Gln1177del
NM_001353765.1:c.315_329del	NP_001340694.1:p.Lys105_Gln109del
XM_024452778.1:c.672_686del	XP_024308546.1:p.Lys224_Gln228del
XM_024452779.1:c.315_329del	XP_024308547.1:p.Lys105_Gln109del
NM_004304.5:c.3519_3533del MANE Select	NP_004295.2:p.Lys1173_Gln1177del
NM_001353765.2:c.315_329del	NP_001340694.1:p.Lys105_Gln109del