Canonical Allele Identifier: CA2765920491
Gene: CPLANE1 HGNC NCBI
CPLANE1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.37249393_37249394insACA , CM000667.2:g.37249393_37249394insACA GRCh38
NC_000005.9:g.37249495_37249496insACA , CM000667.1:g.37249495_37249496insACA GRCh37
NC_000005.8:g.37285252_37285253insACA NCBI36
NG_032772.1:g.5035_5036insTGT
NG_032772.2:g.5035_5036insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000425232.6:c.-197_-196insTGT (CPLANE1) ENSP00000389014.2:n.-197_-196insTGT
NM_023073.3:c.-197_-196insTGT (CPLANE1) NP_075561.3:n.-197_-196insTGT
XR_925921.1:n.171+172_171+173insACA (CPLANE1-AS1)
NR_134263.1:n.176+172_176+173insACA (CPLANE1-AS1)
XM_005248345.4:c.-197_-196insTGT (CPLANE1) XP_005248402.1:n.-197_-196insTGT
XM_005248346.4:c.-197_-196insTGT (CPLANE1) XP_005248403.1:n.-197_-196insTGT
XM_005248347.4:c.-197_-196insTGT (CPLANE1) XP_005248404.1:n.-197_-196insTGT
XM_005248349.4:c.-197_-196insTGT (CPLANE1) XP_005248406.1:n.-197_-196insTGT
XM_005248350.4:c.-197_-196insTGT (CPLANE1) XP_005248407.1:n.-197_-196insTGT
XM_011514087.2:c.-197_-196insTGT (CPLANE1) XP_011512389.1:n.-197_-196insTGT
XM_011514088.2:c.-197_-196insTGT (CPLANE1) XP_011512390.1:n.-197_-196insTGT
XM_011514089.2:c.-197_-196insTGT (CPLANE1) XP_011512391.1:n.-197_-196insTGT
XM_011514092.2:c.-197_-196insTGT (CPLANE1) XP_011512394.1:n.-197_-196insTGT
XR_001742208.1:n.28_29insTGT (CPLANE1)
XR_002956171.1:n.28_29insTGT (CPLANE1)
XR_925644.2:n.28_29insTGT (CPLANE1)