Canonical Allele Identifier: CA2625651069
Gene: VSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259813_74259814insAGGGGCAGGACC , CM000676.2:g.74259813_74259814insAGGGGCAGGACC GRCh38
NC_000014.8:g.74726516_74726517insAGGGGCAGGACC , CM000676.1:g.74726516_74726517insAGGGGCAGGACC GRCh37
NC_000014.7:g.73796269_73796270insAGGGGCAGGACC NCBI36
NG_013092.1:g.25342_25343insAGGGGCAGGACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+31_760+32insAGGGGCAGGACC MANE Select ENSP00000261980.2:n.760+31_760+32insAGGGGCAGGACC
ENST00000261980.2:c.760+31_760+32insAGGGGCAGGACC ENSP00000261980.2:n.760+31_760+32insAGGGGCAGGACC
NM_182894.2:c.760+31_760+32insAGGGGCAGGACC NP_878314.1:n.760+31_760+32insAGGGGCAGGACC
XM_011536719.1:c.760+31_760+32insAGGGGCAGGACC XP_011535021.1:n.760+31_760+32insAGGGGCAGGACC
NM_182894.3:c.760+31_760+32insAGGGGCAGGACC MANE Select NP_878314.1:n.760+31_760+32insAGGGGCAGGACC