Canonical Allele Identifier: CA2406435765
Community Standard Title: NM_024821.5(CCDC134):c.565-2846A=
Gene: CCDC134 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41822852A= , CM000684.2:g.41822852A= GRCh38
NC_000022.10:g.42218856A= , CM000684.1:g.42218856A= GRCh37
NC_000022.9:g.40548802A= NCBI36
NG_068430.1:g.27174A=

Transcript Alleles

HGVS Amino-acid Change
NM_024821.5:c.565-2846A= MANE Select NP_079097.1:n.565-2846A=
ENST00000255784.6:c.565-2846A= MANE Select ENSP00000255784.5:n.565-2846A=
NM_001304797.1:c.226-2846A= NP_001291726.1:n.226-2846A=
NM_001304797.2:c.226-2846A= NP_001291726.1:n.226-2846A=
NM_001382346.1:c.565-2846A= NP_001369275.1:n.565-2846A=
NM_024821.3:c.565-2846A= NP_079097.1:n.565-2846A=
NM_024821.4:c.565-2846A= NP_079097.1:n.565-2846A=
ENST00000255784.5:c.565-2846A= ENSP00000255784.5:n.565-2846A=
ENST00000402061.7:c.226-2846A= ENSP00000385803.3:n.226-2846A=
XM_005261748.2:c.565-2846A= XP_005261805.1:n.565-2846A=
XM_005261748.3:c.565-2846A= XP_005261805.1:n.565-2846A=