Canonical Allele Identifier: CA346462206

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 1376816
• ClinVar RCV Id: RCV001888181
• dbSNP Id: rs758625575
• MyVariant Identifiers: chr2:g.29416547G>C (hg19) ; chr2:g.29193681G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193681G>C , CM000664.2:g.29193681G>C	GRCh38
NC_000002.11:g.29416547G>C , CM000664.1:g.29416547G>C	GRCh37
NC_000002.10:g.29270051G>C	NCBI36
NG_009445.1:g.732886C>G , LRG_488:g.732886C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3247G>C (CLIP4)	ENSP00000508948.1:n.1923-3247G>C
ENST00000389048.8:c.4406C>G (ALK) MANE Select	ENSP00000373700.3:p.Pro1469Arg
ENST00000431873.6:c.1633C>G (ALK)
ENST00000638605.1:n.1283C>G (ALK)
ENST00000642122.1:c.1202C>G (ALK)	ENSP00000493203.1:p.Pro401Arg
ENST00000389048.7:c.4406C>G (ALK)	ENSP00000373700.3:p.Pro1469Arg
ENST00000431873.5:c.1286C>G (ALK)	ENSP00000414027.2:p.Pro429Arg
ENST00000618119.4:c.3275C>G (ALK)	ENSP00000482733.1:p.Pro1092Arg
NM_004304.4:c.4406C>G (ALK)	NP_004295.2:p.Pro1469Arg
NM_001353765.1:c.1202C>G (ALK)	NP_001340694.1:p.Pro401Arg
XM_024452778.1:c.1559C>G (ALK)	XP_024308546.1:p.Pro520Arg
XM_024452779.1:c.1202C>G (ALK)	XP_024308547.1:p.Pro401Arg
NM_004304.5:c.4406C>G (ALK) MANE Select	NP_004295.2:p.Pro1469Arg
NM_001353765.2:c.1202C>G (ALK)	NP_001340694.1:p.Pro401Arg