Canonical Allele Identifier: CA468852421
Gene: ODAD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.28151498A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27862569A>G , CM000672.2:g.27862569A>G GRCh38
NC_000010.10:g.28151498A>G , CM000672.1:g.28151498A>G GRCh37
NC_000010.9:g.28191504A>G NCBI36
NG_042820.1:g.141482T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305242.10:c.2664T>C MANE Select ENSP00000306410.5:p.Asn888=
ENST00000672841.1:c.1740T>C ENSP00000499983.1:p.Asn580=
ENST00000672877.1:c.1239T>C ENSP00000500120.1:p.Asn413=
ENST00000673384.1:c.1740T>C ENSP00000500856.1:p.Asn580=
ENST00000673439.1:c.2664T>C ENSP00000500782.1:p.Asn888=
ENST00000305242.9:c.2664T>C ENSP00000306410.5:p.Asn888=
NM_001290020.1:c.2664T>C NP_001276949.1:p.Asn888=
NM_001290021.1:c.1239T>C NP_001276950.1:p.Asn413=
NM_001312689.1:c.1740T>C NP_001299618.1:p.Asn580=
NM_018076.3:c.2664T>C NP_060546.2:p.Asn888=
NM_018076.4:c.2664T>C NP_060546.2:p.Asn888=
XM_011519526.1:c.2664T>C XP_011517828.1:p.Asn888=
XM_011519527.1:c.2664T>C XP_011517829.1:p.Asn888=
XM_011519528.1:c.2664T>C XP_011517830.1:p.Asn888=
XM_011519529.1:c.2664T>C XP_011517831.1:p.Asn888=
XM_011519530.1:c.2664T>C XP_011517832.1:p.Asn888=
XM_011519531.1:c.2664T>C XP_011517833.1:p.Asn888=
XM_011519532.1:c.2454T>C XP_011517834.1:p.Asn818=
XM_011519533.1:c.1740T>C XP_011517835.1:p.Asn580=
XM_011519534.1:c.1740T>C XP_011517836.1:p.Asn580=
XM_011519535.1:c.1578T>C XP_011517837.1:p.Asn526=
XM_011519537.1:c.1239T>C XP_011517839.1:p.Asn413=
XM_024448049.1:c.2793T>C XP_024303817.1:p.Asn931=
XM_024448050.1:c.2793T>C XP_024303818.1:p.Asn931=
XM_024448051.1:c.2793T>C XP_024303819.1:p.Asn931=
XM_024448052.1:c.2793T>C XP_024303820.1:p.Asn931=
XM_024448053.1:c.2793T>C XP_024303821.1:p.Asn931=
XM_024448054.1:c.2583T>C XP_024303822.1:p.Asn861=
XM_024448055.1:c.1869T>C XP_024303823.1:p.Asn623=
XM_024448056.1:c.1869T>C XP_024303824.1:p.Asn623=
XM_024448057.1:c.1707T>C XP_024303825.1:p.Asn569=
XM_024448058.1:c.1368T>C XP_024303826.1:p.Asn456=
NM_001290020.2:c.2664T>C NP_001276949.1:p.Asn888=
NM_001290021.2:c.1239T>C NP_001276950.1:p.Asn413=
NM_001312689.2:c.1740T>C NP_001299618.1:p.Asn580=
NM_018076.5:c.2664T>C MANE Select NP_060546.2:p.Asn888=