Canonical Allele Identifier: CA964715456
Gene: VSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259815_74259816insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC , CM000676.2:g.74259815_74259816insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC GRCh38
NC_000014.8:g.74726518_74726519insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC , CM000676.1:g.74726518_74726519insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC GRCh37
NC_000014.7:g.73796271_73796272insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC NCBI36
NG_013092.1:g.25344_25345insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC MANE Select ENSP00000261980.2:n.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGC...
ENST00000261980.2:c.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC ENSP00000261980.2:n.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGC...
NM_182894.2:c.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC NP_878314.1:n.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGCTACTGG...
XM_011536719.1:c.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC XP_011535021.1:n.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGCTAC...
NM_182894.3:c.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGCTACTGGGTAAGAGCCCGCACCCTCCTTGGGGTCCTGCCCC MANE Select NP_878314.1:n.760+33_760+34insCTGCAGGACTCCTGTGCCCCGTGGCTACTGG...