Canonical Allele Identifier: CA468852434

Gene: ODAD2

Linked Data

• gnomAD v4: 10-27862575-A-G
• MyVariant Identifiers: chr10:g.28151504A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862575A>G , CM000672.2:g.27862575A>G	GRCh38
NC_000010.10:g.28151504A>G , CM000672.1:g.28151504A>G	GRCh37
NC_000010.9:g.28191510A>G	NCBI36
NG_042820.1:g.141476T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2658T>C MANE Select	ENSP00000306410.5:p.Ile886=
ENST00000672841.1:c.1734T>C	ENSP00000499983.1:p.Ile578=
ENST00000672877.1:c.1233T>C	ENSP00000500120.1:p.Ile411=
ENST00000673384.1:c.1734T>C	ENSP00000500856.1:p.Ile578=
ENST00000673439.1:c.2658T>C	ENSP00000500782.1:p.Ile886=
ENST00000305242.9:c.2658T>C	ENSP00000306410.5:p.Ile886=
NM_001290020.1:c.2658T>C	NP_001276949.1:p.Ile886=
NM_001290021.1:c.1233T>C	NP_001276950.1:p.Ile411=
NM_001312689.1:c.1734T>C	NP_001299618.1:p.Ile578=
NM_018076.3:c.2658T>C	NP_060546.2:p.Ile886=
NM_018076.4:c.2658T>C	NP_060546.2:p.Ile886=
XM_011519526.1:c.2658T>C	XP_011517828.1:p.Ile886=
XM_011519527.1:c.2658T>C	XP_011517829.1:p.Ile886=
XM_011519528.1:c.2658T>C	XP_011517830.1:p.Ile886=
XM_011519529.1:c.2658T>C	XP_011517831.1:p.Ile886=
XM_011519530.1:c.2658T>C	XP_011517832.1:p.Ile886=
XM_011519531.1:c.2658T>C	XP_011517833.1:p.Ile886=
XM_011519532.1:c.2448T>C	XP_011517834.1:p.Ile816=
XM_011519533.1:c.1734T>C	XP_011517835.1:p.Ile578=
XM_011519534.1:c.1734T>C	XP_011517836.1:p.Ile578=
XM_011519535.1:c.1572T>C	XP_011517837.1:p.Ile524=
XM_011519537.1:c.1233T>C	XP_011517839.1:p.Ile411=
XM_024448049.1:c.2787T>C	XP_024303817.1:p.Ile929=
XM_024448050.1:c.2787T>C	XP_024303818.1:p.Ile929=
XM_024448051.1:c.2787T>C	XP_024303819.1:p.Ile929=
XM_024448052.1:c.2787T>C	XP_024303820.1:p.Ile929=
XM_024448053.1:c.2787T>C	XP_024303821.1:p.Ile929=
XM_024448054.1:c.2577T>C	XP_024303822.1:p.Ile859=
XM_024448055.1:c.1863T>C	XP_024303823.1:p.Ile621=
XM_024448056.1:c.1863T>C	XP_024303824.1:p.Ile621=
XM_024448057.1:c.1701T>C	XP_024303825.1:p.Ile567=
XM_024448058.1:c.1362T>C	XP_024303826.1:p.Ile454=
NM_001290020.2:c.2658T>C	NP_001276949.1:p.Ile886=
NM_001290021.2:c.1233T>C	NP_001276950.1:p.Ile411=
NM_001312689.2:c.1734T>C	NP_001299618.1:p.Ile578=
NM_018076.5:c.2658T>C MANE Select	NP_060546.2:p.Ile886=