Canonical Allele Identifier: CA425618773

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193227G>C , CM000664.2:g.29193227G>C	GRCh38
NC_000002.11:g.29416093G>C , CM000664.1:g.29416093G>C	GRCh37
NC_000002.10:g.29269597G>C	NCBI36
NG_009445.1:g.733340C>G , LRG_488:g.733340C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3701G>C (CLIP4)	ENSP00000508948.1:n.1923-3701G>C
ENST00000389048.8:c.4860C>G (ALK) MANE Select	ENSP00000373700.3:p.Pro1620=
ENST00000431873.6:c.2087C>G (ALK)
ENST00000638605.1:n.1737C>G (ALK)
ENST00000642122.1:c.1656C>G (ALK)	ENSP00000493203.1:p.Pro552=
ENST00000389048.7:c.4860C>G (ALK)	ENSP00000373700.3:p.Pro1620=
ENST00000431873.5:c.1740C>G (ALK)	ENSP00000414027.2:p.Pro580=
ENST00000618119.4:c.3729C>G (ALK)	ENSP00000482733.1:p.Pro1243=
NM_004304.4:c.4860C>G (ALK)	NP_004295.2:p.Pro1620=
NM_001353765.1:c.1656C>G (ALK)	NP_001340694.1:p.Pro552=
XM_024452778.1:c.2013C>G (ALK)	XP_024308546.1:p.Pro671=
XM_024452779.1:c.1656C>G (ALK)	XP_024308547.1:p.Pro552=
NM_004304.5:c.4860C>G (ALK) MANE Select	NP_004295.2:p.Pro1620=
NM_001353765.2:c.1656C>G (ALK)	NP_001340694.1:p.Pro552=