Canonical Allele Identifier: CA425619226

Linked Data

dbSNP Id: rs2148138560
gnomAD v4: 2-29193719-G-C
MyVariant Identifiers: chr2:g.29416585G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29193719G>C , CM000664.2:g.29193719G>C GRCh38
NC_000002.11:g.29416585G>C , CM000664.1:g.29416585G>C GRCh37
NC_000002.10:g.29270089G>C NCBI36
NG_009445.1:g.732848C>G , LRG_488:g.732848C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689605.1:c.1923-3209G>C (CLIP4) ENSP00000508948.1:n.1923-3209G>C
ENST00000389048.8:c.4368C>G (ALK) MANE Select ENSP00000373700.3:p.Pro1456=
ENST00000431873.6:c.1595C>G (ALK)
ENST00000638605.1:n.1245C>G (ALK)
ENST00000642122.1:c.1164C>G (ALK) ENSP00000493203.1:p.Pro388=
ENST00000389048.7:c.4368C>G (ALK) ENSP00000373700.3:p.Pro1456=
ENST00000431873.5:c.1248C>G (ALK) ENSP00000414027.2:p.Pro416=
ENST00000618119.4:c.3237C>G (ALK) ENSP00000482733.1:p.Pro1079=
NM_004304.4:c.4368C>G (ALK) NP_004295.2:p.Pro1456=
NM_001353765.1:c.1164C>G (ALK) NP_001340694.1:p.Pro388=
XM_024452778.1:c.1521C>G (ALK) XP_024308546.1:p.Pro507=
XM_024452779.1:c.1164C>G (ALK) XP_024308547.1:p.Pro388=
NM_004304.5:c.4368C>G (ALK) MANE Select NP_004295.2:p.Pro1456=
NM_001353765.2:c.1164C>G (ALK) NP_001340694.1:p.Pro388=