Canonical Allele Identifier: CA366030300

Gene: IYD

Linked Data

• MyVariant Identifiers: chr6:g.150710578C>A (hg19) ; chr6:g.150389442C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389442C>A , CM000668.2:g.150389442C>A	GRCh38
NC_000006.11:g.150710578C>A , CM000668.1:g.150710578C>A	GRCh37
NC_000006.10:g.150752271C>A	NCBI36
NG_016007.1:g.25551C>A
NG_016007.2:g.25551C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344419.8:c.269C>A MANE Select	ENSP00000343763.4:p.Ser90Tyr
ENST00000229447.9:c.269C>A	ENSP00000229447.5:p.Ser90Tyr
ENST00000344419.7:c.269C>A	ENSP00000343763.3:p.Ser90Tyr
ENST00000367335.7:c.269C>A	ENSP00000356304.3:p.Ser90Tyr
ENST00000392255.7:c.269C>A	ENSP00000376084.3:p.Ser90Tyr
ENST00000392256.6:c.269C>A	ENSP00000376085.2:p.Ser90Tyr
ENST00000422583.2:c.146C>A	ENSP00000397342.2:p.Ser49Tyr
ENST00000425615.3:c.104C>A	ENSP00000390081.3:p.Ser35Tyr
ENST00000500320.7:c.269C>A	ENSP00000441276.1:p.Ser90Tyr
ENST00000546121.1:n.212C>A
NM_001164694.1:c.269C>A	NP_001158166.1:p.Ser90Tyr
NM_001164695.1:c.269C>A	NP_001158167.1:p.Ser90Tyr
NM_203395.2:c.269C>A	NP_981932.1:p.Ser90Tyr
XM_006715478.2:c.269C>A	XP_006715541.1:p.Ser90Tyr
XM_006715479.2:c.104C>A	XP_006715542.1:p.Ser35Tyr
XR_245516.3:n.432C>A
NM_001318495.1:c.91C>A	NP_001305424.1:p.Leu31Ile
NR_134655.1:n.409C>A
XM_006715478.3:c.269C>A	XP_006715541.1:p.Ser90Tyr
XM_006715479.3:c.104C>A	XP_006715542.1:p.Ser35Tyr
NM_001164694.2:c.269C>A	NP_001158166.1:p.Ser90Tyr
NM_001164695.2:c.269C>A	NP_001158167.1:p.Ser90Tyr
NM_001318495.2:c.91C>A	NP_001305424.1:p.Leu31Ile
NM_203395.3:c.269C>A MANE Select	NP_981932.1:p.Ser90Tyr
NR_134655.2:n.289C>A