Canonical Allele Identifier: CA1593482

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193301C>T , CM000664.2:g.29193301C>T	GRCh38
NC_000002.11:g.29416167C>T , CM000664.1:g.29416167C>T	GRCh37
NC_000002.10:g.29269671C>T	NCBI36
NG_009445.1:g.733266G>A , LRG_488:g.733266G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4786G>A (ALK) MANE Select	NP_004295.2:p.Ala1596Thr
ENST00000389048.8:c.4786G>A (ALK) MANE Select	ENSP00000373700.3:p.Ala1596Thr
NM_001353765.1:c.1582G>A (ALK)	NP_001340694.1:p.Ala528Thr
NM_001353765.2:c.1582G>A (ALK)	NP_001340694.1:p.Ala528Thr
NM_004304.4:c.4786G>A (ALK)	NP_004295.2:p.Ala1596Thr
ENST00000389048.7:c.4786G>A (ALK)	ENSP00000373700.3:p.Ala1596Thr
ENST00000431873.5:c.1666G>A (ALK)	ENSP00000414027.2:p.Ala556Thr
ENST00000431873.6:c.2013G>A (ALK)
ENST00000618119.4:c.3655G>A (ALK)	ENSP00000482733.1:p.Ala1219Thr
ENST00000638605.1:n.1663G>A (ALK)
ENST00000642122.1:c.1582G>A (ALK)	ENSP00000493203.1:p.Ala528Thr
ENST00000689605.1:c.1923-3627C>T (CLIP4)	ENSP00000508948.1:n.1923-3627C>T
XM_024452778.1:c.1939G>A (ALK)	XP_024308546.1:p.Ala647Thr
XM_024452779.1:c.1582G>A (ALK)	XP_024308547.1:p.Ala528Thr