Canonical Allele Identifier: CA592783490

Gene: ODAD2

Linked Data

• dbSNP Id: rs1217872182
• gnomAD v2: 10-28151476-CTTT-C
• gnomAD v3: 10-27862547-CTTT-C
• gnomAD v4: 10-27862547-CTTT-C
• MyVariant Identifiers: chr10:g.28151477_28151479del (hg19) ; chr10:g.27862548_27862550del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.27862548_27862550del , CM000672.2:g.27862548_27862550del	GRCh38
NC_000010.10:g.28151477_28151479del , CM000672.1:g.28151477_28151479del	GRCh37
NC_000010.9:g.28191483_28191485del	NCBI36
NG_042820.1:g.141501_141503del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305242.10:c.2683_2685del MANE Select	ENSP00000306410.5:p.Lys895del
ENST00000672841.1:c.1759_1761del	ENSP00000499983.1:p.Lys587del
ENST00000672877.1:c.1258_1260del	ENSP00000500120.1:p.Lys420del
ENST00000673384.1:c.1759_1761del	ENSP00000500856.1:p.Lys587del
ENST00000673439.1:c.2683_2685del	ENSP00000500782.1:p.Lys895del
ENST00000305242.9:c.2683_2685del	ENSP00000306410.5:p.Lys895del
NM_001290020.1:c.2683_2685del	NP_001276949.1:p.Lys895del
NM_001290021.1:c.1258_1260del	NP_001276950.1:p.Lys420del
NM_001312689.1:c.1759_1761del	NP_001299618.1:p.Lys587del
NM_018076.3:c.2683_2685del	NP_060546.2:p.Lys895del
NM_018076.4:c.2683_2685del	NP_060546.2:p.Lys895del
XM_011519526.1:c.2683_2685del	XP_011517828.1:p.Lys895del
XM_011519527.1:c.2683_2685del	XP_011517829.1:p.Lys895del
XM_011519528.1:c.2683_2685del	XP_011517830.1:p.Lys895del
XM_011519529.1:c.2683_2685del	XP_011517831.1:p.Lys895del
XM_011519530.1:c.2683_2685del	XP_011517832.1:p.Lys895del
XM_011519531.1:c.2683_2685del	XP_011517833.1:p.Lys895del
XM_011519532.1:c.2473_2475del	XP_011517834.1:p.Lys825del
XM_011519533.1:c.1759_1761del	XP_011517835.1:p.Lys587del
XM_011519534.1:c.1759_1761del	XP_011517836.1:p.Lys587del
XM_011519535.1:c.1597_1599del	XP_011517837.1:p.Lys533del
XM_011519537.1:c.1258_1260del	XP_011517839.1:p.Lys420del
XM_024448049.1:c.2812_2814del	XP_024303817.1:p.Lys938del
XM_024448050.1:c.2812_2814del	XP_024303818.1:p.Lys938del
XM_024448051.1:c.2812_2814del	XP_024303819.1:p.Lys938del
XM_024448052.1:c.2812_2814del	XP_024303820.1:p.Lys938del
XM_024448053.1:c.2812_2814del	XP_024303821.1:p.Lys938del
XM_024448054.1:c.2602_2604del	XP_024303822.1:p.Lys868del
XM_024448055.1:c.1888_1890del	XP_024303823.1:p.Lys630del
XM_024448056.1:c.1888_1890del	XP_024303824.1:p.Lys630del
XM_024448057.1:c.1726_1728del	XP_024303825.1:p.Lys576del
XM_024448058.1:c.1387_1389del	XP_024303826.1:p.Lys463del
NM_001290020.2:c.2683_2685del	NP_001276949.1:p.Lys895del
NM_001290021.2:c.1258_1260del	NP_001276950.1:p.Lys420del
NM_001312689.2:c.1759_1761del	NP_001299618.1:p.Lys587del
NM_018076.5:c.2683_2685del MANE Select	NP_060546.2:p.Lys895del