Canonical Allele Identifier: CA1241071061

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193622A= , CM000664.2:g.29193622A=	GRCh38
NC_000002.11:g.29416488A= , CM000664.1:g.29416488A=	GRCh37
NC_000002.10:g.29269992A=	NCBI36
NG_009445.1:g.732945T= , LRG_488:g.732945T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3306A= (CLIP4)	ENSP00000508948.1:n.1923-3306A=
ENST00000389048.8:c.4465T= (ALK) MANE Select	ENSP00000373700.3:p.Leu1489=
ENST00000431873.6:c.1692T= (ALK)
ENST00000638605.1:n.1342T= (ALK)
ENST00000642122.1:c.1261T= (ALK)	ENSP00000493203.1:p.Leu421=
ENST00000389048.7:c.4465T= (ALK)	ENSP00000373700.3:p.Leu1489=
ENST00000431873.5:c.1345T= (ALK)	ENSP00000414027.2:p.Leu449=
ENST00000618119.4:c.3334T= (ALK)	ENSP00000482733.1:p.Leu1112=
NM_004304.4:c.4465T= (ALK)	NP_004295.2:p.Leu1489=
NM_001353765.1:c.1261T= (ALK)	NP_001340694.1:p.Leu421=
XM_024452778.1:c.1618T= (ALK)	XP_024308546.1:p.Leu540=
XM_024452779.1:c.1261T= (ALK)	XP_024308547.1:p.Leu421=
NM_004304.5:c.4465T= (ALK) MANE Select	NP_004295.2:p.Leu1489=
NM_001353765.2:c.1261T= (ALK)	NP_001340694.1:p.Leu421=