Canonical Allele Identifier: CA2625651067
Gene: VSX2 HGNC NCBI

Linked Data

gnomAD v4: 14-74259811-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259811_74259812insA , CM000676.2:g.74259811_74259812insA GRCh38
NC_000014.8:g.74726514_74726515insA , CM000676.1:g.74726514_74726515insA GRCh37
NC_000014.7:g.73796267_73796268insA NCBI36
NG_013092.1:g.25340_25341insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+29_760+30insA MANE Select ENSP00000261980.2:n.760+29_760+30insA
ENST00000261980.2:c.760+29_760+30insA ENSP00000261980.2:n.760+29_760+30insA
NM_182894.2:c.760+29_760+30insA NP_878314.1:n.760+29_760+30insA
XM_011536719.1:c.760+29_760+30insA XP_011535021.1:n.760+29_760+30insA
NM_182894.3:c.760+29_760+30insA MANE Select NP_878314.1:n.760+29_760+30insA
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