Canonical Allele Identifier: CA346460026

Gene: CLIP4 ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29193242C>A , CM000664.2:g.29193242C>A	GRCh38
NC_000002.11:g.29416108C>A , CM000664.1:g.29416108C>A	GRCh37
NC_000002.10:g.29269612C>A	NCBI36
NG_009445.1:g.733325G>T , LRG_488:g.733325G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004304.5:c.4845G>T (ALK) MANE Select	NP_004295.2:p.Met1615Ile
ENST00000389048.8:c.4845G>T (ALK) MANE Select	ENSP00000373700.3:p.Met1615Ile
NM_001353765.1:c.1641G>T (ALK)	NP_001340694.1:p.Met547Ile
NM_001353765.2:c.1641G>T (ALK)	NP_001340694.1:p.Met547Ile
NM_004304.4:c.4845G>T (ALK)	NP_004295.2:p.Met1615Ile
ENST00000389048.7:c.4845G>T (ALK)	ENSP00000373700.3:p.Met1615Ile
ENST00000431873.5:c.1725G>T (ALK)	ENSP00000414027.2:p.Met575Ile
ENST00000431873.6:c.2072G>T (ALK)
ENST00000618119.4:c.3714G>T (ALK)	ENSP00000482733.1:p.Met1238Ile
ENST00000638605.1:n.1722G>T (ALK)
ENST00000642122.1:c.1641G>T (ALK)	ENSP00000493203.1:p.Met547Ile
ENST00000689605.1:c.1923-3686C>A (CLIP4)	ENSP00000508948.1:n.1923-3686C>A
XM_024452778.1:c.1998G>T (ALK)	XP_024308546.1:p.Met666Ile
XM_024452779.1:c.1641G>T (ALK)	XP_024308547.1:p.Met547Ile