Canonical Allele Identifier: CA1828292643

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729392_2729395delinsTCTC , CM000671.2:g.2729392_2729395delinsTCTC GRCh38
NC_000009.11:g.2729392_2729395delinsTCTC , CM000671.1:g.2729392_2729395delinsTCTC GRCh37
NC_000009.10:g.2719392_2719395delinsTCTC NCBI36
NG_012181.1:g.16867_16870delinsTCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1357-54_1357-51delinsTCTC (KCNV2) MANE Select ENSP00000371514.3:n.1357-54_1357-51delins...
ENST00000382082.3:c.1357-54_1357-51delinsTCTC (KCNV2) ENSP00000371514.3:n.1357-54_1357-51delins...
ENST00000490444.2:c.277-8863_277-8860delinsGAGA (PUM3) ENSP00000474467.1:n.277-8863_277-8860deli...
NM_133497.3:c.1357-54_1357-51delinsTCTC (KCNV2) NP_598004.1:n.1357-54_1357-51delinsTCTC
XR_929202.1:n.2002-54_2002-51delinsTCTC (KCNV2)
XR_929203.1:n.2368_2371delinsTCTC (KCNV2)
NM_133497.4:c.1357-54_1357-51delinsTCTC (KCNV2) MANE Select NP_598004.1:n.1357-54_1357-51delinsTCTC