Canonical Allele Identifier: CA2689245779

Linked Data

gnomAD v4: 9-2729685-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729686del , CM000671.2:g.2729686del GRCh38
NC_000009.11:g.2729686del , CM000671.1:g.2729686del GRCh37
NC_000009.10:g.2719686del NCBI36
NG_012181.1:g.17161del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.1597del (KCNV2) MANE Select ENSP00000371514.3:p.Gly534GlufsTer16
ENST00000382082.3:c.1597del (KCNV2) ENSP00000371514.3:p.Gly534GlufsTer16
ENST00000490444.2:c.277-9154del (PUM3) ENSP00000474467.1:n.277-9154del
NM_133497.3:c.1597del (KCNV2) NP_598004.1:p.Gly534GlufsTer16
NM_133497.4:c.1597del (KCNV2) MANE Select NP_598004.1:p.Gly534GlufsTer16