Canonical Allele Identifier: CA452567449

Gene: IYD

Linked Data

• gnomAD v4: 6-150389458-A-G
• MyVariant Identifiers: chr6:g.150710594A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389458A>G , CM000668.2:g.150389458A>G	GRCh38
NC_000006.11:g.150710594A>G , CM000668.1:g.150710594A>G	GRCh37
NC_000006.10:g.150752287A>G	NCBI36
NG_016007.1:g.25567A>G
NG_016007.2:g.25567A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.285A>G MANE Select	ENSP00000343763.4:p.Glu95=
ENST00000229447.9:c.285A>G	ENSP00000229447.5:p.Glu95=
ENST00000344419.7:c.285A>G	ENSP00000343763.3:p.Glu95=
ENST00000367335.7:c.285A>G	ENSP00000356304.3:p.Glu95=
ENST00000392255.7:c.285A>G	ENSP00000376084.3:p.Glu95=
ENST00000392256.6:c.285A>G	ENSP00000376085.2:p.Glu95=
ENST00000422583.2:c.162A>G	ENSP00000397342.2:p.Glu54=
ENST00000425615.3:c.120A>G	ENSP00000390081.3:p.Glu40=
ENST00000500320.7:c.285A>G	ENSP00000441276.1:p.Glu95=
ENST00000546121.1:n.228A>G
NM_001164694.1:c.285A>G	NP_001158166.1:p.Glu95=
NM_001164695.1:c.285A>G	NP_001158167.1:p.Glu95=
NM_203395.2:c.285A>G	NP_981932.1:p.Glu95=
XM_006715478.2:c.285A>G	XP_006715541.1:p.Glu95=
XM_006715479.2:c.120A>G	XP_006715542.1:p.Glu40=
XR_245516.3:n.448A>G
NM_001318495.1:c.107A>G	NP_001305424.1:p.Asn36Ser
NR_134655.1:n.425A>G
XM_006715478.3:c.285A>G	XP_006715541.1:p.Glu95=
XM_006715479.3:c.120A>G	XP_006715542.1:p.Glu40=
NM_001164694.2:c.285A>G	NP_001158166.1:p.Glu95=
NM_001164695.2:c.285A>G	NP_001158167.1:p.Glu95=
NM_001318495.2:c.107A>G	NP_001305424.1:p.Asn36Ser
NM_203395.3:c.285A>G MANE Select	NP_981932.1:p.Glu95=
NR_134655.2:n.305A>G