Canonical Allele Identifier: CA1095800356

Gene: IYD

Linked Data

• dbSNP Id: rs1778424319
• gnomAD v3: 6-150398912-G-GTA
• gnomAD v4: 6-150398912-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398913_150398914dup , CM000668.2:g.150398913_150398914dup	GRCh38
NC_000006.11:g.150720049_150720050dup , CM000668.1:g.150720049_150720050dup	GRCh37
NC_000006.10:g.150761742_150761743dup	NCBI36
NG_016007.1:g.35022_35023dup
NG_016007.2:g.35022_35023dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*676_*677dup MANE Select	ENSP00000343763.4:n.*676_*677dup
ENST00000229447.9:c.*776_*777dup	ENSP00000229447.5:n.*776_*777dup
ENST00000344419.7:c.*676_*677dup	ENSP00000343763.3:n.*676_*677dup
NM_001164694.1:c.*776_*777dup	NP_001158166.1:n.*776_*777dup
NM_001164695.1:c.*863_*864dup	NP_001158167.1:n.*863_*864dup
NM_203395.2:c.*676_*677dup	NP_981932.1:n.*676_*677dup
NM_001318495.1:c.*676_*677dup	NP_001305424.1:n.*676_*677dup
NR_134655.1:n.1859_1860dup
NM_001164694.2:c.*776_*777dup	NP_001158166.1:n.*776_*777dup
NM_001164695.2:c.*863_*864dup	NP_001158167.1:n.*863_*864dup
NM_001318495.2:c.*676_*677dup	NP_001305424.1:n.*676_*677dup
NM_203395.3:c.*676_*677dup MANE Select	NP_981932.1:n.*676_*677dup
NR_134655.2:n.1739_1740dup