Canonical Allele Identifier: CA1828293248

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729679G= , CM000671.2:g.2729679G= GRCh38
NC_000009.11:g.2729679G= , CM000671.1:g.2729679G= GRCh37
NC_000009.10:g.2719679G= NCBI36
NG_012181.1:g.17154G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.1590G= (KCNV2) MANE Select ENSP00000371514.3:p.Glu530=
ENST00000382082.3:c.1590G= (KCNV2) ENSP00000371514.3:p.Glu530=
ENST00000490444.2:c.277-9147C= (PUM3) ENSP00000474467.1:n.277-9147C=
NM_133497.3:c.1590G= (KCNV2) NP_598004.1:p.Glu530=
NM_133497.4:c.1590G= (KCNV2) MANE Select NP_598004.1:p.Glu530=