Canonical Allele Identifier: CA2658457960

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29193628_29193630del , CM000664.2:g.29193628_29193630del GRCh38
NC_000002.11:g.29416494_29416496del , CM000664.1:g.29416494_29416496del GRCh37
NC_000002.10:g.29269998_29270000del NCBI36
NG_009445.1:g.732938_732940del , LRG_488:g.732938_732940del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689605.1:c.1923-3300_1923-3298del (CLIP4) ENSP00000508948.1:n.1923-3300_1923-3298del
ENST00000389048.8:c.4458_4460del (ALK) MANE Select ENSP00000373700.3:p.Ser1487del
ENST00000431873.6:c.1685_1687del (ALK)
ENST00000638605.1:n.1335_1337del (ALK)
ENST00000642122.1:c.1254_1256del (ALK) ENSP00000493203.1:p.Ser419del
ENST00000389048.7:c.4458_4460del (ALK) ENSP00000373700.3:p.Ser1487del
ENST00000431873.5:c.1338_1340del (ALK) ENSP00000414027.2:p.Ser447del
ENST00000618119.4:c.3327_3329del (ALK) ENSP00000482733.1:p.Ser1110del
NM_004304.4:c.4458_4460del (ALK) NP_004295.2:p.Ser1487del
NM_001353765.1:c.1254_1256del (ALK) NP_001340694.1:p.Ser419del
XM_024452778.1:c.1611_1613del (ALK) XP_024308546.1:p.Ser538del
XM_024452779.1:c.1254_1256del (ALK) XP_024308547.1:p.Ser419del
NM_004304.5:c.4458_4460del (ALK) MANE Select NP_004295.2:p.Ser1487del
NM_001353765.2:c.1254_1256del (ALK) NP_001340694.1:p.Ser419del