Canonical Allele Identifier: CA1139656813

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193615_29193616delinsCG , CM000664.2:g.29193615_29193616delinsCG	GRCh38
NC_000002.11:g.29416481_29416482delinsCG , CM000664.1:g.29416481_29416482delinsCG	GRCh37
NC_000002.10:g.29269985_29269986delinsCG	NCBI36
NG_009445.1:g.732951_732952delinsCG , LRG_488:g.732951_732952delinsCG

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4471_4472delinsCG (ALK) MANE Select	NP_004295.2:p.Lys1491Arg
ENST00000389048.8:c.4471_4472delinsCG (ALK) MANE Select	ENSP00000373700.3:p.Lys1491Arg
NM_001353765.1:c.1267_1268delinsCG (ALK)	NP_001340694.1:p.Lys423Arg
NM_001353765.2:c.1267_1268delinsCG (ALK)	NP_001340694.1:p.Lys423Arg
NM_004304.4:c.4471_4472delinsCG (ALK)	NP_004295.2:p.Lys1491Arg
ENST00000389048.7:c.4471_4472delinsCG (ALK)	ENSP00000373700.3:p.Lys1491Arg
ENST00000431873.5:c.1351_1352delinsCG (ALK)	ENSP00000414027.2:p.Lys451Arg
ENST00000431873.6:c.1698_1699delinsCG (ALK)
ENST00000618119.4:c.3340_3341delinsCG (ALK)	ENSP00000482733.1:p.Lys1114Arg
ENST00000638605.1:n.1348_1349delinsCG (ALK)
ENST00000642122.1:c.1267_1268delinsCG (ALK)	ENSP00000493203.1:p.Lys423Arg
ENST00000689605.1:c.1923-3313_1923-3312delinsCG (CLIP4)	ENSP00000508948.1:n.1923-3313_1923-3312delinsCG
XM_024452778.1:c.1624_1625delinsCG (ALK)	XP_024308546.1:p.Lys542Arg
XM_024452779.1:c.1267_1268delinsCG (ALK)	XP_024308547.1:p.Lys423Arg