Canonical Allele Identifier: CA1828292627

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729383T= , CM000671.2:g.2729383T= GRCh38
NC_000009.11:g.2729383T= , CM000671.1:g.2729383T= GRCh37
NC_000009.10:g.2719383T= NCBI36
NG_012181.1:g.16858T=

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1357-63T= (KCNV2) MANE Select ENSP00000371514.3:n.1357-63T=
ENST00000382082.3:c.1357-63T= (KCNV2) ENSP00000371514.3:n.1357-63T=
ENST00000490444.2:c.277-8851A= (PUM3) ENSP00000474467.1:n.277-8851A=
NM_133497.3:c.1357-63T= (KCNV2) NP_598004.1:n.1357-63T=
XR_929202.1:n.2002-63T= (KCNV2)
XR_929203.1:n.2359T= (KCNV2)
NM_133497.4:c.1357-63T= (KCNV2) MANE Select NP_598004.1:n.1357-63T=