Canonical Allele Identifier: CA862771014

Linked Data

dbSNP Id: rs1209060192

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729397_2729399del , CM000671.2:g.2729397_2729399del GRCh38
NC_000009.11:g.2729397_2729399del , CM000671.1:g.2729397_2729399del GRCh37
NC_000009.10:g.2719397_2719399del NCBI36
NG_012181.1:g.16872_16874del

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1357-49_1357-47del (KCNV2) MANE Select ENSP00000371514.3:n.1357-49_1357-47del
ENST00000382082.3:c.1357-49_1357-47del (KCNV2) ENSP00000371514.3:n.1357-49_1357-47del
ENST00000490444.2:c.277-8863_277-8861del (PUM3) ENSP00000474467.1:n.277-8863_277-8861del
NM_133497.3:c.1357-49_1357-47del (KCNV2) NP_598004.1:n.1357-49_1357-47del
XR_929202.1:n.2002-49_2002-47del (KCNV2)
XR_929203.1:n.2373_2375del (KCNV2)
NM_133497.4:c.1357-49_1357-47del (KCNV2) MANE Select NP_598004.1:n.1357-49_1357-47del