Canonical Allele Identifier: CA2689246882
Gene: KCNV2 HGNC NCBI

Linked Data

gnomAD v4: 9-2718560-T-TG

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718562dup , CM000671.2:g.2718562dup GRCh38
NC_000009.11:g.2718562dup , CM000671.1:g.2718562dup GRCh37
NC_000009.10:g.2708562dup NCBI36
NG_012181.1:g.6037dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.823dup MANE Select ENSP00000371514.3:p.Val275GlyfsTer?
ENST00000382082.3:c.823dup ENSP00000371514.3:p.Val275GlyfsTer?
NM_133497.3:c.823dup NP_598004.1:p.Val275GlyfsTer?
XR_929202.1:n.1324dup
XR_929203.1:n.1324dup
NM_133497.4:c.823dup MANE Select NP_598004.1:p.Val275GlyfsTer?