Canonical Allele Identifier: CA2782688102
Gene: KCNV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718552_2718563del , CM000671.2:g.2718552_2718563del GRCh38
NC_000009.11:g.2718552_2718563del , CM000671.1:g.2718552_2718563del GRCh37
NC_000009.10:g.2708552_2708563del NCBI36
NG_012181.1:g.6027_6038del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.813_824del MANE Select ENSP00000371514.3:p.Val272_Val275del
ENST00000382082.3:c.813_824del ENSP00000371514.3:p.Val272_Val275del
NM_133497.3:c.813_824del NP_598004.1:p.Val272_Val275del
XR_929202.1:n.1314_1325del
XR_929203.1:n.1314_1325del
NM_133497.4:c.813_824del MANE Select NP_598004.1:p.Val272_Val275del