Canonical Allele Identifier: CA366029825

Gene: IYD

Linked Data

• MyVariant Identifiers: chr6:g.150710515A>T (hg19) ; chr6:g.150389379A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389379A>T , CM000668.2:g.150389379A>T	GRCh38
NC_000006.11:g.150710515A>T , CM000668.1:g.150710515A>T	GRCh37
NC_000006.10:g.150752208A>T	NCBI36
NG_016007.1:g.25488A>T
NG_016007.2:g.25488A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.206A>T MANE Select	ENSP00000343763.4:p.Glu69Val
ENST00000229447.9:c.206A>T	ENSP00000229447.5:p.Glu69Val
ENST00000344419.7:c.206A>T	ENSP00000343763.3:p.Glu69Val
ENST00000367335.7:c.206A>T	ENSP00000356304.3:p.Glu69Val
ENST00000392255.7:c.206A>T	ENSP00000376084.3:p.Glu69Val
ENST00000392256.6:c.206A>T	ENSP00000376085.2:p.Glu69Val
ENST00000422583.2:c.83A>T	ENSP00000397342.2:p.Glu28Val
ENST00000425615.3:c.41A>T	ENSP00000390081.3:p.Glu14Val
ENST00000500320.7:c.206A>T	ENSP00000441276.1:p.Glu69Val
ENST00000546121.1:n.149A>T
NM_001164694.1:c.206A>T	NP_001158166.1:p.Glu69Val
NM_001164695.1:c.206A>T	NP_001158167.1:p.Glu69Val
NM_203395.2:c.206A>T	NP_981932.1:p.Glu69Val
XM_006715478.2:c.206A>T	XP_006715541.1:p.Glu69Val
XM_006715479.2:c.41A>T	XP_006715542.1:p.Glu14Val
XR_245516.3:n.369A>T
NM_001318495.1:c.28A>T	NP_001305424.1:p.Lys10Ter
NR_134655.1:n.346A>T
XM_006715478.3:c.206A>T	XP_006715541.1:p.Glu69Val
XM_006715479.3:c.41A>T	XP_006715542.1:p.Glu14Val
NM_001164694.2:c.206A>T	NP_001158166.1:p.Glu69Val
NM_001164695.2:c.206A>T	NP_001158167.1:p.Glu69Val
NM_001318495.2:c.28A>T	NP_001305424.1:p.Lys10Ter
NM_203395.3:c.206A>T MANE Select	NP_981932.1:p.Glu69Val
NR_134655.2:n.226A>T