Canonical Allele Identifier: CA2689245395

Linked Data

gnomAD v4: 9-2729397-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729397T>A , CM000671.2:g.2729397T>A GRCh38
NC_000009.11:g.2729397T>A , CM000671.1:g.2729397T>A GRCh37
NC_000009.10:g.2719397T>A NCBI36
NG_012181.1:g.16872T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1357-49T>A (KCNV2) MANE Select ENSP00000371514.3:n.1357-49T>A
ENST00000382082.3:c.1357-49T>A (KCNV2) ENSP00000371514.3:n.1357-49T>A
ENST00000490444.2:c.277-8865A>T (PUM3) ENSP00000474467.1:n.277-8865A>T
NM_133497.3:c.1357-49T>A (KCNV2) NP_598004.1:n.1357-49T>A
XR_929202.1:n.2002-49T>A (KCNV2)
XR_929203.1:n.2373T>A (KCNV2)
NM_133497.4:c.1357-49T>A (KCNV2) MANE Select NP_598004.1:n.1357-49T>A