Canonical Allele Identifier: CA425619135

Gene: CLIP4 ALK

Linked Data

• MyVariant Identifiers: chr2:g.29416531T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193665T>A , CM000664.2:g.29193665T>A	GRCh38
NC_000002.11:g.29416531T>A , CM000664.1:g.29416531T>A	GRCh37
NC_000002.10:g.29270035T>A	NCBI36
NG_009445.1:g.732902A>T , LRG_488:g.732902A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689605.1:c.1923-3263T>A (CLIP4)	ENSP00000508948.1:n.1923-3263T>A
ENST00000389048.8:c.4422A>T (ALK) MANE Select	ENSP00000373700.3:p.Gly1474=
ENST00000431873.6:c.1649A>T (ALK)
ENST00000638605.1:n.1299A>T (ALK)
ENST00000642122.1:c.1218A>T (ALK)	ENSP00000493203.1:p.Gly406=
ENST00000389048.7:c.4422A>T (ALK)	ENSP00000373700.3:p.Gly1474=
ENST00000431873.5:c.1302A>T (ALK)	ENSP00000414027.2:p.Gly434=
ENST00000618119.4:c.3291A>T (ALK)	ENSP00000482733.1:p.Gly1097=
NM_004304.4:c.4422A>T (ALK)	NP_004295.2:p.Gly1474=
NM_001353765.1:c.1218A>T (ALK)	NP_001340694.1:p.Gly406=
XM_024452778.1:c.1575A>T (ALK)	XP_024308546.1:p.Gly525=
XM_024452779.1:c.1218A>T (ALK)	XP_024308547.1:p.Gly406=
NM_004304.5:c.4422A>T (ALK) MANE Select	NP_004295.2:p.Gly1474=
NM_001353765.2:c.1218A>T (ALK)	NP_001340694.1:p.Gly406=