Canonical Allele Identifier: CA1593577

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193676C>T , CM000664.2:g.29193676C>T	GRCh38
NC_000002.11:g.29416542C>T , CM000664.1:g.29416542C>T	GRCh37
NC_000002.10:g.29270046C>T	NCBI36
NG_009445.1:g.732891G>A , LRG_488:g.732891G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4411G>A (ALK) MANE Select	NP_004295.2:p.Val1471Met
ENST00000389048.8:c.4411G>A (ALK) MANE Select	ENSP00000373700.3:p.Val1471Met
NM_001353765.1:c.1207G>A (ALK)	NP_001340694.1:p.Val403Met
NM_001353765.2:c.1207G>A (ALK)	NP_001340694.1:p.Val403Met
NM_004304.4:c.4411G>A (ALK)	NP_004295.2:p.Val1471Met
ENST00000389048.7:c.4411G>A (ALK)	ENSP00000373700.3:p.Val1471Met
ENST00000431873.5:c.1291G>A (ALK)	ENSP00000414027.2:p.Val431Met
ENST00000431873.6:c.1638G>A (ALK)
ENST00000618119.4:c.3280G>A (ALK)	ENSP00000482733.1:p.Val1094Met
ENST00000638605.1:n.1288G>A (ALK)
ENST00000642122.1:c.1207G>A (ALK)	ENSP00000493203.1:p.Val403Met
ENST00000689605.1:c.1923-3252C>T (CLIP4)	ENSP00000508948.1:n.1923-3252C>T
XM_024452778.1:c.1564G>A (ALK)	XP_024308546.1:p.Val522Met
XM_024452779.1:c.1207G>A (ALK)	XP_024308547.1:p.Val403Met