Canonical Allele Identifier: CA1828293433

Linked Data

dbSNP Id: rs1820038079

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729769del , CM000671.2:g.2729769del GRCh38
NC_000009.11:g.2729769del , CM000671.1:g.2729769del GRCh37
NC_000009.10:g.2719769del NCBI36
NG_012181.1:g.17244del

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.*42del (KCNV2) MANE Select ENSP00000371514.3:n.*42del
ENST00000382082.3:c.*42del (KCNV2) ENSP00000371514.3:n.*42del
ENST00000490444.2:c.277-9236del (PUM3) ENSP00000474467.1:n.277-9236del
NM_133497.3:c.*42del (KCNV2) NP_598004.1:n.*42del
NM_133497.4:c.*42del (KCNV2) MANE Select NP_598004.1:n.*42del