Canonical Allele Identifier: CA2608644748
Gene: ODAD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27862440_27862442dup , CM000672.2:g.27862440_27862442dup GRCh38
NC_000010.10:g.28151369_28151371dup , CM000672.1:g.28151369_28151371dup GRCh37
NC_000010.9:g.28191375_28191377dup NCBI36
NG_042820.1:g.141609_141611dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000305242.10:c.2791_2793dup MANE Select ENSP00000306410.5:p.Ala931_Asn932insAla
ENST00000672841.1:c.1867_1869dup ENSP00000499983.1:p.Ala623_Asn624insAla
ENST00000672877.1:c.1366_1368dup ENSP00000500120.1:p.Ala456_Asn457insAla
ENST00000673384.1:c.1867_1869dup ENSP00000500856.1:p.Ala623_Asn624insAla
ENST00000673439.1:c.2791_2793dup ENSP00000500782.1:p.Ala931_Asn932insAla
ENST00000305242.9:c.2791_2793dup ENSP00000306410.5:p.Ala931_Asn932insAla
NM_001290020.1:c.2791_2793dup NP_001276949.1:p.Ala931_Asn932insAla
NM_001290021.1:c.1366_1368dup NP_001276950.1:p.Ala456_Asn457insAla
NM_001312689.1:c.1867_1869dup NP_001299618.1:p.Ala623_Asn624insAla
NM_018076.3:c.2791_2793dup NP_060546.2:p.Ala931_Asn932insAla
NM_018076.4:c.2791_2793dup NP_060546.2:p.Ala931_Asn932insAla
XM_011519526.1:c.2791_2793dup XP_011517828.1:p.Ala931_Asn932insAla
XM_011519527.1:c.2791_2793dup XP_011517829.1:p.Ala931_Asn932insAla
XM_011519528.1:c.2791_2793dup XP_011517830.1:p.Ala931_Asn932insAla
XM_011519529.1:c.2791_2793dup XP_011517831.1:p.Ala931_Asn932insAla
XM_011519530.1:c.2791_2793dup XP_011517832.1:p.Ala931_Asn932insAla
XM_011519531.1:c.2791_2793dup XP_011517833.1:p.Ala931_Asn932insAla
XM_011519532.1:c.2581_2583dup XP_011517834.1:p.Ala861_Asn862insAla
XM_011519533.1:c.1867_1869dup XP_011517835.1:p.Ala623_Asn624insAla
XM_011519534.1:c.1867_1869dup XP_011517836.1:p.Ala623_Asn624insAla
XM_011519535.1:c.1705_1707dup XP_011517837.1:p.Ala569_Asn570insAla
XM_011519537.1:c.1366_1368dup XP_011517839.1:p.Ala456_Asn457insAla
XM_024448049.1:c.2920_2922dup XP_024303817.1:p.Ala974_Asn975insAla
XM_024448050.1:c.2920_2922dup XP_024303818.1:p.Ala974_Asn975insAla
XM_024448051.1:c.2920_2922dup XP_024303819.1:p.Ala974_Asn975insAla
XM_024448052.1:c.2920_2922dup XP_024303820.1:p.Ala974_Asn975insAla
XM_024448053.1:c.2920_2922dup XP_024303821.1:p.Ala974_Asn975insAla
XM_024448054.1:c.2710_2712dup XP_024303822.1:p.Ala904_Asn905insAla
XM_024448055.1:c.1996_1998dup XP_024303823.1:p.Ala666_Asn667insAla
XM_024448056.1:c.1996_1998dup XP_024303824.1:p.Ala666_Asn667insAla
XM_024448057.1:c.1834_1836dup XP_024303825.1:p.Ala612_Asn613insAla
XM_024448058.1:c.1495_1497dup XP_024303826.1:p.Ala499_Asn500insAla
NM_001290020.2:c.2791_2793dup NP_001276949.1:p.Ala931_Asn932insAla
NM_001290021.2:c.1366_1368dup NP_001276950.1:p.Ala456_Asn457insAla
NM_001312689.2:c.1867_1869dup NP_001299618.1:p.Ala623_Asn624insAla
NM_018076.5:c.2791_2793dup MANE Select NP_060546.2:p.Ala931_Asn932insAla