Canonical Allele Identifier: CA4965319
Gene: KCNV2 HGNC NCBI

Linked Data

dbSNP Id: rs769260522

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717859_2717869del , CM000671.2:g.2717859_2717869del GRCh38
NC_000009.11:g.2717859_2717869del , CM000671.1:g.2717859_2717869del GRCh37
NC_000009.10:g.2707859_2707869del NCBI36
NG_012181.1:g.5334_5344del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.120_130del MANE Select ENSP00000371514.3:p.Ala41ArgfsTer8
ENST00000382082.3:c.120_130del ENSP00000371514.3:p.Ala41ArgfsTer8
NM_133497.3:c.120_130del NP_598004.1:p.Ala41ArgfsTer8
XR_929202.1:n.621_631del
XR_929203.1:n.621_631del
NM_133497.4:c.120_130del MANE Select NP_598004.1:p.Ala41ArgfsTer8