Canonical Allele Identifier: CA425433958

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs2148143670
• MyVariant Identifiers: chr2:g.29420539G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197673G>T , CM000664.2:g.29197673G>T	GRCh38
NC_000002.11:g.29420539G>T , CM000664.1:g.29420539G>T	GRCh37
NC_000002.10:g.29274043G>T	NCBI36
NG_009445.1:g.728894C>A , LRG_488:g.728894C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*667G>T (CLIP4)	ENSP00000508948.1:n.*667G>T
ENST00000389048.8:c.3942C>A (ALK) MANE Select	ENSP00000373700.3:p.Ser1314=
ENST00000431873.6:c.1169C>A (ALK)
ENST00000638605.1:n.819C>A (ALK)
ENST00000642122.1:c.738C>A (ALK)	ENSP00000493203.1:p.Ser246=
ENST00000389048.7:c.3942C>A (ALK)	ENSP00000373700.3:p.Ser1314=
ENST00000431873.5:c.822C>A (ALK)	ENSP00000414027.2:p.Ser274=
ENST00000618119.4:c.2811C>A (ALK)	ENSP00000482733.1:p.Ser937=
NM_004304.4:c.3942C>A (ALK)	NP_004295.2:p.Ser1314=
NM_001353765.1:c.738C>A (ALK)	NP_001340694.1:p.Ser246=
XM_024452778.1:c.1095C>A (ALK)	XP_024308546.1:p.Ser365=
XM_024452779.1:c.738C>A (ALK)	XP_024308547.1:p.Ser246=
NM_004304.5:c.3942C>A (ALK) MANE Select	NP_004295.2:p.Ser1314=
NM_001353765.2:c.738C>A (ALK)	NP_001340694.1:p.Ser246=