Canonical Allele Identifier: CA2625651034
Gene: VSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259572_74259575del , CM000676.2:g.74259572_74259575del GRCh38
NC_000014.8:g.74726275_74726278del , CM000676.1:g.74726275_74726278del GRCh37
NC_000014.7:g.73796028_73796031del NCBI36
NG_013092.1:g.25101_25104del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.580-30_580-27del MANE Select ENSP00000261980.2:n.580-30_580-27del
ENST00000261980.2:c.580-30_580-27del ENSP00000261980.2:n.580-30_580-27del
NM_182894.2:c.580-30_580-27del NP_878314.1:n.580-30_580-27del
XM_011536719.1:c.580-30_580-27del XP_011535021.1:n.580-30_580-27del
NM_182894.3:c.580-30_580-27del MANE Select NP_878314.1:n.580-30_580-27del