Canonical Allele Identifier: CA1593502

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193363C>G , CM000664.2:g.29193363C>G	GRCh38
NC_000002.11:g.29416229C>G , CM000664.1:g.29416229C>G	GRCh37
NC_000002.10:g.29269733C>G	NCBI36
NG_009445.1:g.733204G>C , LRG_488:g.733204G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4724G>C (ALK) MANE Select	NP_004295.2:p.Arg1575Pro
ENST00000389048.8:c.4724G>C (ALK) MANE Select	ENSP00000373700.3:p.Arg1575Pro
NM_001353765.1:c.1520G>C (ALK)	NP_001340694.1:p.Arg507Pro
NM_001353765.2:c.1520G>C (ALK)	NP_001340694.1:p.Arg507Pro
NM_004304.4:c.4724G>C (ALK)	NP_004295.2:p.Arg1575Pro
ENST00000389048.7:c.4724G>C (ALK)	ENSP00000373700.3:p.Arg1575Pro
ENST00000431873.5:c.1604G>C (ALK)	ENSP00000414027.2:p.Arg535Pro
ENST00000431873.6:c.1951G>C (ALK)
ENST00000618119.4:c.3593G>C (ALK)	ENSP00000482733.1:p.Arg1198Pro
ENST00000638605.1:n.1601G>C (ALK)
ENST00000642122.1:c.1520G>C (ALK)	ENSP00000493203.1:p.Arg507Pro
ENST00000689605.1:c.1923-3565C>G (CLIP4)	ENSP00000508948.1:n.1923-3565C>G
XM_024452778.1:c.1877G>C (ALK)	XP_024308546.1:p.Arg626Pro
XM_024452779.1:c.1520G>C (ALK)	XP_024308547.1:p.Arg507Pro