Canonical Allele Identifier: CA1593613

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193850C>T , CM000664.2:g.29193850C>T	GRCh38
NC_000002.11:g.29416716C>T , CM000664.1:g.29416716C>T	GRCh37
NC_000002.10:g.29270220C>T	NCBI36
NG_009445.1:g.732717G>A , LRG_488:g.732717G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4237G>A (ALK) MANE Select	NP_004295.2:p.Val1413Met
ENST00000389048.8:c.4237G>A (ALK) MANE Select	ENSP00000373700.3:p.Val1413Met
NM_001353765.1:c.1033G>A (ALK)	NP_001340694.1:p.Val345Met
NM_001353765.2:c.1033G>A (ALK)	NP_001340694.1:p.Val345Met
NM_004304.4:c.4237G>A (ALK)	NP_004295.2:p.Val1413Met
ENST00000389048.7:c.4237G>A (ALK)	ENSP00000373700.3:p.Val1413Met
ENST00000431873.5:c.1117G>A (ALK)	ENSP00000414027.2:p.Val373Met
ENST00000431873.6:c.1464G>A (ALK)
ENST00000618119.4:c.3106G>A (ALK)	ENSP00000482733.1:p.Val1036Met
ENST00000638605.1:n.1114G>A (ALK)
ENST00000642122.1:c.1033G>A (ALK)	ENSP00000493203.1:p.Val345Met
ENST00000689605.1:c.1923-3078C>T (CLIP4)	ENSP00000508948.1:n.1923-3078C>T
XM_024452778.1:c.1390G>A (ALK)	XP_024308546.1:p.Val464Met
XM_024452779.1:c.1033G>A (ALK)	XP_024308547.1:p.Val345Met