Canonical Allele Identifier: CA1828292631

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2729385_2729389delinsCCTTT , CM000671.2:g.2729385_2729389delinsCCTTT GRCh38
NC_000009.11:g.2729385_2729389delinsCCTTT , CM000671.1:g.2729385_2729389delinsCCTTT GRCh37
NC_000009.10:g.2719385_2719389delinsCCTTT NCBI36
NG_012181.1:g.16860_16864delinsCCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.1357-61_1357-57delinsCCTTT (KCNV2) MANE Select ENSP00000371514.3:n.1357-61_1357-57delins...
ENST00000382082.3:c.1357-61_1357-57delinsCCTTT (KCNV2) ENSP00000371514.3:n.1357-61_1357-57delins...
ENST00000490444.2:c.277-8857_277-8853delinsAAAGG (PUM3) ENSP00000474467.1:n.277-8857_277-8853deli...
NM_133497.3:c.1357-61_1357-57delinsCCTTT (KCNV2) NP_598004.1:n.1357-61_1357-57delinsCCTTT
XR_929202.1:n.2002-61_2002-57delinsCCTTT (KCNV2)
XR_929203.1:n.2361_2365delinsCCTTT (KCNV2)
NM_133497.4:c.1357-61_1357-57delinsCCTTT (KCNV2) MANE Select NP_598004.1:n.1357-61_1357-57delinsCCTTT