Canonical Allele Identifier: CA346462550

Gene: CLIP4 ALK

Linked Data

• ClinVar Variation Id: 470871
• ClinVar RCV Id: RCV000530604 ; RCV003153720
• dbSNP Id: rs1553387094
• MyVariant Identifiers: chr2:g.29416610G>A (hg19) ; chr2:g.29193744G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193744G>A , CM000664.2:g.29193744G>A	GRCh38
NC_000002.11:g.29416610G>A , CM000664.1:g.29416610G>A	GRCh37
NC_000002.10:g.29270114G>A	NCBI36
NG_009445.1:g.732823C>T , LRG_488:g.732823C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3184G>A (CLIP4)	ENSP00000508948.1:n.1923-3184G>A
ENST00000389048.8:c.4343C>T (ALK) MANE Select	ENSP00000373700.3:p.Ser1448Phe
ENST00000431873.6:c.1570C>T (ALK)
ENST00000638605.1:n.1220C>T (ALK)
ENST00000642122.1:c.1139C>T (ALK)	ENSP00000493203.1:p.Ser380Phe
ENST00000389048.7:c.4343C>T (ALK)	ENSP00000373700.3:p.Ser1448Phe
ENST00000431873.5:c.1223C>T (ALK)	ENSP00000414027.2:p.Ser408Phe
ENST00000618119.4:c.3212C>T (ALK)	ENSP00000482733.1:p.Ser1071Phe
NM_004304.4:c.4343C>T (ALK)	NP_004295.2:p.Ser1448Phe
NM_001353765.1:c.1139C>T (ALK)	NP_001340694.1:p.Ser380Phe
XM_024452778.1:c.1496C>T (ALK)	XP_024308546.1:p.Ser499Phe
XM_024452779.1:c.1139C>T (ALK)	XP_024308547.1:p.Ser380Phe
NM_004304.5:c.4343C>T (ALK) MANE Select	NP_004295.2:p.Ser1448Phe
NM_001353765.2:c.1139C>T (ALK)	NP_001340694.1:p.Ser380Phe