Canonical Allele Identifier: CA3063902897

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193704_29193706delinsAAC , CM000664.2:g.29193704_29193706delinsAAC	GRCh38
NC_000002.11:g.29416570_29416572delinsAAC , CM000664.1:g.29416570_29416572delinsAAC	GRCh37
NC_000002.10:g.29270074_29270076delinsAAC	NCBI36
NG_009445.1:g.732861_732863delinsGTT , LRG_488:g.732861_732863delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3224_1923-3222delinsAAC (CLIP4)	ENSP00000508948.1:n.1923-3224_1923-3222delinsAAC
ENST00000389048.8:c.4381_4383delinsGTT (ALK) MANE Select	ENSP00000373700.3:p.Ile1461Val
ENST00000431873.6:c.1608_1610delinsGTT (ALK)
ENST00000638605.1:n.1258_1260delinsGTT (ALK)
ENST00000642122.1:c.1177_1179delinsGTT (ALK)	ENSP00000493203.1:p.Ile393Val
ENST00000389048.7:c.4381_4383delinsGTT (ALK)	ENSP00000373700.3:p.Ile1461Val
ENST00000431873.5:c.1261_1263delinsGTT (ALK)	ENSP00000414027.2:p.Ile421Val
ENST00000618119.4:c.3250_3252delinsGTT (ALK)	ENSP00000482733.1:p.Ile1084Val
NM_004304.4:c.4381_4383delinsGTT (ALK)	NP_004295.2:p.Ile1461Val
NM_001353765.1:c.1177_1179delinsGTT (ALK)	NP_001340694.1:p.Ile393Val
XM_024452778.1:c.1534_1536delinsGTT (ALK)	XP_024308546.1:p.Ile512Val
XM_024452779.1:c.1177_1179delinsGTT (ALK)	XP_024308547.1:p.Ile393Val
NM_004304.5:c.4381_4383delinsGTT (ALK) MANE Select	NP_004295.2:p.Ile1461Val
NM_001353765.2:c.1177_1179delinsGTT (ALK)	NP_001340694.1:p.Ile393Val