Canonical Allele Identifier: CA531464413

Gene: CLIP4 ALK

Linked Data

• dbSNP Id: rs1365906513
• gnomAD v2: 2-29420013-G-C
• gnomAD v3: 2-29197147-G-C
• gnomAD v4: 2-29197147-G-C
• MyVariant Identifiers: chr2:g.29420013G>C (hg19) ; chr2:g.29197147G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29197147G>C , CM000664.2:g.29197147G>C	GRCh38
NC_000002.11:g.29420013G>C , CM000664.1:g.29420013G>C	GRCh37
NC_000002.10:g.29273517G>C	NCBI36
NG_009445.1:g.729420C>G , LRG_488:g.729420C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.*141G>C (CLIP4)	ENSP00000508948.1:n.*141G>C
ENST00000389048.8:c.4074-287C>G (ALK) MANE Select	ENSP00000373700.3:n.4074-287C>G
ENST00000431873.6:c.1301-287C>G (ALK)
ENST00000638605.1:n.951-287C>G (ALK)
ENST00000642122.1:c.870-287C>G (ALK)	ENSP00000493203.1:n.870-287C>G
ENST00000389048.7:c.4074-287C>G (ALK)	ENSP00000373700.3:n.4074-287C>G
ENST00000431873.5:c.954-287C>G (ALK)	ENSP00000414027.2:n.954-287C>G
ENST00000618119.4:c.2943-287C>G (ALK)	ENSP00000482733.1:n.2943-287C>G
NM_004304.4:c.4074-287C>G (ALK)	NP_004295.2:n.4074-287C>G
NM_001353765.1:c.870-287C>G (ALK)	NP_001340694.1:n.870-287C>G
XM_024452778.1:c.1227-287C>G (ALK)	XP_024308546.1:n.1227-287C>G
XM_024452779.1:c.870-287C>G (ALK)	XP_024308547.1:n.870-287C>G
NM_004304.5:c.4074-287C>G (ALK) MANE Select	NP_004295.2:n.4074-287C>G
NM_001353765.2:c.870-287C>G (ALK)	NP_001340694.1:n.870-287C>G