Canonical Allele Identifier: CA44634750

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193397C>T , CM000664.2:g.29193397C>T	GRCh38
NC_000002.11:g.29416263C>T , CM000664.1:g.29416263C>T	GRCh37
NC_000002.10:g.29269767C>T	NCBI36
NG_009445.1:g.733170G>A , LRG_488:g.733170G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4690G>A (ALK) MANE Select	NP_004295.2:p.Ala1564Thr
ENST00000389048.8:c.4690G>A (ALK) MANE Select	ENSP00000373700.3:p.Ala1564Thr
NM_001353765.1:c.1486G>A (ALK)	NP_001340694.1:p.Ala496Thr
NM_001353765.2:c.1486G>A (ALK)	NP_001340694.1:p.Ala496Thr
NM_004304.4:c.4690G>A (ALK)	NP_004295.2:p.Ala1564Thr
ENST00000389048.7:c.4690G>A (ALK)	ENSP00000373700.3:p.Ala1564Thr
ENST00000431873.5:c.1570G>A (ALK)	ENSP00000414027.2:p.Ala524Thr
ENST00000431873.6:c.1917G>A (ALK)
ENST00000618119.4:c.3559G>A (ALK)	ENSP00000482733.1:p.Ala1187Thr
ENST00000638605.1:n.1567G>A (ALK)
ENST00000642122.1:c.1486G>A (ALK)	ENSP00000493203.1:p.Ala496Thr
ENST00000689605.1:c.1923-3531C>T (CLIP4)	ENSP00000508948.1:n.1923-3531C>T
XM_024452778.1:c.1843G>A (ALK)	XP_024308546.1:p.Ala615Thr
XM_024452779.1:c.1486G>A (ALK)	XP_024308547.1:p.Ala496Thr