Canonical Allele Identifier: CA2689246010

Linked Data

gnomAD v4: 9-2729789-T-TA

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729791dup , CM000671.2:g.2729791dup GRCh38
NC_000009.11:g.2729791dup , CM000671.1:g.2729791dup GRCh37
NC_000009.10:g.2719791dup NCBI36
NG_012181.1:g.17266dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.*64dup (KCNV2) MANE Select ENSP00000371514.3:n.*64dup
ENST00000382082.3:c.*64dup (KCNV2) ENSP00000371514.3:n.*64dup
ENST00000490444.2:c.277-9258dup (PUM3) ENSP00000474467.1:n.277-9258dup
NM_133497.3:c.*64dup (KCNV2) NP_598004.1:n.*64dup
NM_133497.4:c.*64dup (KCNV2) MANE Select NP_598004.1:n.*64dup