Canonical Allele Identifier: CA753285430

Gene: CCDC134

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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