Canonical Allele Identifier: CA44634764

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193402A>C , CM000664.2:g.29193402A>C	GRCh38
NC_000002.11:g.29416268A>C , CM000664.1:g.29416268A>C	GRCh37
NC_000002.10:g.29269772A>C	NCBI36
NG_009445.1:g.733165T>G , LRG_488:g.733165T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4685T>G (ALK) MANE Select	NP_004295.2:p.Leu1562Arg
ENST00000389048.8:c.4685T>G (ALK) MANE Select	ENSP00000373700.3:p.Leu1562Arg
NM_001353765.1:c.1481T>G (ALK)	NP_001340694.1:p.Leu494Arg
NM_001353765.2:c.1481T>G (ALK)	NP_001340694.1:p.Leu494Arg
NM_004304.4:c.4685T>G (ALK)	NP_004295.2:p.Leu1562Arg
ENST00000389048.7:c.4685T>G (ALK)	ENSP00000373700.3:p.Leu1562Arg
ENST00000431873.5:c.1565T>G (ALK)	ENSP00000414027.2:p.Leu522Arg
ENST00000431873.6:c.1912T>G (ALK)
ENST00000618119.4:c.3554T>G (ALK)	ENSP00000482733.1:p.Leu1185Arg
ENST00000638605.1:n.1562T>G (ALK)
ENST00000642122.1:c.1481T>G (ALK)	ENSP00000493203.1:p.Leu494Arg
ENST00000689605.1:c.1923-3526A>C (CLIP4)	ENSP00000508948.1:n.1923-3526A>C
XM_024452778.1:c.1838T>G (ALK)	XP_024308546.1:p.Leu613Arg
XM_024452779.1:c.1481T>G (ALK)	XP_024308547.1:p.Leu494Arg