Canonical Allele Identifier: CA346462632

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 1739722
• ClinVar RCV Id: RCV002332059
• dbSNP Id: rs80004824
• MyVariant Identifiers: chr2:g.29416629G>A (hg19) ; chr2:g.29193763G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193763G>A , CM000664.2:g.29193763G>A	GRCh38
NC_000002.11:g.29416629G>A , CM000664.1:g.29416629G>A	GRCh37
NC_000002.10:g.29270133G>A	NCBI36
NG_009445.1:g.732804C>T , LRG_488:g.732804C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3165G>A (CLIP4)	ENSP00000508948.1:n.1923-3165G>A
ENST00000389048.8:c.4324C>T (ALK) MANE Select	ENSP00000373700.3:p.Pro1442Ser
ENST00000431873.6:c.1551C>T (ALK)
ENST00000638605.1:n.1201C>T (ALK)
ENST00000642122.1:c.1120C>T (ALK)	ENSP00000493203.1:p.Pro374Ser
ENST00000389048.7:c.4324C>T (ALK)	ENSP00000373700.3:p.Pro1442Ser
ENST00000431873.5:c.1204C>T (ALK)	ENSP00000414027.2:p.Pro402Ser
ENST00000618119.4:c.3193C>T (ALK)	ENSP00000482733.1:p.Pro1065Ser
NM_004304.4:c.4324C>T (ALK)	NP_004295.2:p.Pro1442Ser
NM_001353765.1:c.1120C>T (ALK)	NP_001340694.1:p.Pro374Ser
XM_024452778.1:c.1477C>T (ALK)	XP_024308546.1:p.Pro493Ser
XM_024452779.1:c.1120C>T (ALK)	XP_024308547.1:p.Pro374Ser
NM_004304.5:c.4324C>T (ALK) MANE Select	NP_004295.2:p.Pro1442Ser
NM_001353765.2:c.1120C>T (ALK)	NP_001340694.1:p.Pro374Ser