Canonical Allele Identifier: CA372803344

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729474A>C , CM000671.2:g.2729474A>C GRCh38
NC_000009.11:g.2729474A>C , CM000671.1:g.2729474A>C GRCh37
NC_000009.10:g.2719474A>C NCBI36
NG_012181.1:g.16949A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.1385A>C (KCNV2) MANE Select ENSP00000371514.3:p.Asp462Ala
ENST00000382082.3:c.1385A>C (KCNV2) ENSP00000371514.3:p.Asp462Ala
ENST00000490444.2:c.277-8942T>G (PUM3) ENSP00000474467.1:n.277-8942T>G
NM_133497.3:c.1385A>C (KCNV2) NP_598004.1:p.Asp462Ala
XR_929202.1:n.2030A>C (KCNV2)
NM_133497.4:c.1385A>C (KCNV2) MANE Select NP_598004.1:p.Asp462Ala