Canonical Allele Identifier: CA366030812

Gene: IYD

Linked Data

• MyVariant Identifiers: chr6:g.150710661A>G (hg19) ; chr6:g.150389525A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389525A>G , CM000668.2:g.150389525A>G	GRCh38
NC_000006.11:g.150710661A>G , CM000668.1:g.150710661A>G	GRCh37
NC_000006.10:g.150752354A>G	NCBI36
NG_016007.1:g.25634A>G
NG_016007.2:g.25634A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344419.8:c.352A>G MANE Select	ENSP00000343763.4:p.Asn118Asp
ENST00000229447.9:c.352A>G	ENSP00000229447.5:p.Asn118Asp
ENST00000344419.7:c.352A>G	ENSP00000343763.3:p.Asn118Asp
ENST00000367335.7:c.352A>G	ENSP00000356304.3:p.Asn118Asp
ENST00000392255.7:c.352A>G	ENSP00000376084.3:p.Asn118Asp
ENST00000392256.6:c.352A>G	ENSP00000376085.2:p.Asn118Asp
ENST00000422583.2:c.179+50A>G	ENSP00000397342.2:n.179+50A>G
ENST00000425615.3:c.187A>G	ENSP00000390081.3:p.Asn63Asp
ENST00000500320.7:c.352A>G	ENSP00000441276.1:p.Asn118Asp
ENST00000546121.1:n.295A>G
NM_001164694.1:c.352A>G	NP_001158166.1:p.Asn118Asp
NM_001164695.1:c.352A>G	NP_001158167.1:p.Asn118Asp
NM_203395.2:c.352A>G	NP_981932.1:p.Asn118Asp
XM_006715478.2:c.352A>G	XP_006715541.1:p.Asn118Asp
XM_006715479.2:c.187A>G	XP_006715542.1:p.Asn63Asp
XR_245516.3:n.515A>G
NM_001318495.1:c.124+50A>G	NP_001305424.1:n.124+50A>G
NR_134655.1:n.492A>G
XM_006715478.3:c.352A>G	XP_006715541.1:p.Asn118Asp
XM_006715479.3:c.187A>G	XP_006715542.1:p.Asn63Asp
NM_001164694.2:c.352A>G	NP_001158166.1:p.Asn118Asp
NM_001164695.2:c.352A>G	NP_001158167.1:p.Asn118Asp
NM_001318495.2:c.124+50A>G	NP_001305424.1:n.124+50A>G
NM_203395.3:c.352A>G MANE Select	NP_981932.1:p.Asn118Asp
NR_134655.2:n.372A>G