Canonical Allele Identifier: CA425433899

Gene: CLIP4 ALK

Linked Data

• MyVariant Identifiers: chr2:g.29420446T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197580T>G , CM000664.2:g.29197580T>G	GRCh38
NC_000002.11:g.29420446T>G , CM000664.1:g.29420446T>G	GRCh37
NC_000002.10:g.29273950T>G	NCBI36
NG_009445.1:g.728987A>C , LRG_488:g.728987A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*574T>G (CLIP4)	ENSP00000508948.1:n.*574T>G
ENST00000389048.8:c.4035A>C (ALK) MANE Select	ENSP00000373700.3:p.Gly1345=
ENST00000431873.6:c.1262A>C (ALK)
ENST00000638605.1:n.912A>C (ALK)
ENST00000642122.1:c.831A>C (ALK)	ENSP00000493203.1:p.Gly277=
ENST00000389048.7:c.4035A>C (ALK)	ENSP00000373700.3:p.Gly1345=
ENST00000431873.5:c.915A>C (ALK)	ENSP00000414027.2:p.Gly305=
ENST00000618119.4:c.2904A>C (ALK)	ENSP00000482733.1:p.Gly968=
NM_004304.4:c.4035A>C (ALK)	NP_004295.2:p.Gly1345=
NM_001353765.1:c.831A>C (ALK)	NP_001340694.1:p.Gly277=
XM_024452778.1:c.1188A>C (ALK)	XP_024308546.1:p.Gly396=
XM_024452779.1:c.831A>C (ALK)	XP_024308547.1:p.Gly277=
NM_004304.5:c.4035A>C (ALK) MANE Select	NP_004295.2:p.Gly1345=
NM_001353765.2:c.831A>C (ALK)	NP_001340694.1:p.Gly277=