Canonical Allele Identifier: CA205047833

Gene: ODAD2

Linked Data

• dbSNP Id: rs911207095
• gnomAD v3: 10-27862425-GTTAC-G
• gnomAD v4: 10-27862425-GTTAC-G
• MyVariant Identifiers: chr10:g.28151355_28151358del (hg19) ; chr10:g.27862426_27862429del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862431_27862434del , CM000672.2:g.27862431_27862434del	GRCh38
NC_000010.10:g.28151360_28151363del , CM000672.1:g.28151360_28151363del	GRCh37
NC_000010.9:g.28191366_28191369del	NCBI36
NG_042820.1:g.141622_141625del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2799+5_2799+8del
ENST00000672841.1:c.1875+5_1875+8del
ENST00000672877.1:c.1374+5_1374+8del
ENST00000673384.1:c.1875+5_1875+8del
ENST00000673439.1:c.2799+5_2799+8del
ENST00000305242.9:c.2799+5_2799+8del
NM_001290020.1:c.2799+5_2799+8del
NM_001290021.1:c.1374+5_1374+8del
NM_001312689.1:c.1875+5_1875+8del
NM_018076.3:c.2799+5_2799+8del
NM_018076.4:c.2799+5_2799+8del
XM_011519526.1:c.2799+5_2799+8del
XM_011519527.1:c.2799+5_2799+8del
XM_011519528.1:c.2799+5_2799+8del
XM_011519529.1:c.2799+5_2799+8del
XM_011519530.1:c.2799+5_2799+8del
XM_011519531.1:c.2799+5_2799+8del
XM_011519532.1:c.2589+5_2589+8del
XM_011519533.1:c.1875+5_1875+8del
XM_011519534.1:c.1875+5_1875+8del
XM_011519535.1:c.1713+5_1713+8del
XM_011519537.1:c.1374+5_1374+8del
XM_024448049.1:c.2928+5_2928+8del
XM_024448050.1:c.2928+5_2928+8del
XM_024448051.1:c.2928+5_2928+8del
XM_024448052.1:c.2928+5_2928+8del
XM_024448053.1:c.2928+5_2928+8del
XM_024448054.1:c.2718+5_2718+8del
XM_024448055.1:c.2004+5_2004+8del
XM_024448056.1:c.2004+5_2004+8del
XM_024448057.1:c.1842+5_1842+8del
XM_024448058.1:c.1503+5_1503+8del
NM_001290020.2:c.2799+5_2799+8del
NM_001290021.2:c.1374+5_1374+8del
NM_001312689.2:c.1875+5_1875+8del
NM_018076.5:c.2799+5_2799+8del