Canonical Allele Identifier: CA425619214

Gene: CLIP4 ALK

Linked Data

• MyVariant Identifiers: chr2:g.29416576T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193710T>G , CM000664.2:g.29193710T>G	GRCh38
NC_000002.11:g.29416576T>G , CM000664.1:g.29416576T>G	GRCh37
NC_000002.10:g.29270080T>G	NCBI36
NG_009445.1:g.732857A>C , LRG_488:g.732857A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3218T>G (CLIP4)	ENSP00000508948.1:n.1923-3218T>G
ENST00000389048.8:c.4377A>C (ALK) MANE Select	ENSP00000373700.3:p.Ala1459=
ENST00000431873.6:c.1604A>C (ALK)
ENST00000638605.1:n.1254A>C (ALK)
ENST00000642122.1:c.1173A>C (ALK)	ENSP00000493203.1:p.Ala391=
ENST00000389048.7:c.4377A>C (ALK)	ENSP00000373700.3:p.Ala1459=
ENST00000431873.5:c.1257A>C (ALK)	ENSP00000414027.2:p.Ala419=
ENST00000618119.4:c.3246A>C (ALK)	ENSP00000482733.1:p.Ala1082=
NM_004304.4:c.4377A>C (ALK)	NP_004295.2:p.Ala1459=
NM_001353765.1:c.1173A>C (ALK)	NP_001340694.1:p.Ala391=
XM_024452778.1:c.1530A>C (ALK)	XP_024308546.1:p.Ala510=
XM_024452779.1:c.1173A>C (ALK)	XP_024308547.1:p.Ala391=
NM_004304.5:c.4377A>C (ALK) MANE Select	NP_004295.2:p.Ala1459=
NM_001353765.2:c.1173A>C (ALK)	NP_001340694.1:p.Ala391=