Canonical Allele Identifier: CA366030819

Gene: IYD

Linked Data

• MyVariant Identifiers: chr6:g.150710662A>C (hg19) ; chr6:g.150389526A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389526A>C , CM000668.2:g.150389526A>C	GRCh38
NC_000006.11:g.150710662A>C , CM000668.1:g.150710662A>C	GRCh37
NC_000006.10:g.150752355A>C	NCBI36
NG_016007.1:g.25635A>C
NG_016007.2:g.25635A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344419.8:c.353A>C MANE Select	ENSP00000343763.4:p.Asn118Thr
ENST00000229447.9:c.353A>C	ENSP00000229447.5:p.Asn118Thr
ENST00000344419.7:c.353A>C	ENSP00000343763.3:p.Asn118Thr
ENST00000367335.7:c.353A>C	ENSP00000356304.3:p.Asn118Thr
ENST00000392255.7:c.353A>C	ENSP00000376084.3:p.Asn118Thr
ENST00000392256.6:c.353A>C	ENSP00000376085.2:p.Asn118Thr
ENST00000422583.2:c.179+51A>C	ENSP00000397342.2:n.179+51A>C
ENST00000425615.3:c.188A>C	ENSP00000390081.3:p.Asn63Thr
ENST00000500320.7:c.353A>C	ENSP00000441276.1:p.Asn118Thr
ENST00000546121.1:n.296A>C
NM_001164694.1:c.353A>C	NP_001158166.1:p.Asn118Thr
NM_001164695.1:c.353A>C	NP_001158167.1:p.Asn118Thr
NM_203395.2:c.353A>C	NP_981932.1:p.Asn118Thr
XM_006715478.2:c.353A>C	XP_006715541.1:p.Asn118Thr
XM_006715479.2:c.188A>C	XP_006715542.1:p.Asn63Thr
XR_245516.3:n.516A>C
NM_001318495.1:c.124+51A>C	NP_001305424.1:n.124+51A>C
NR_134655.1:n.493A>C
XM_006715478.3:c.353A>C	XP_006715541.1:p.Asn118Thr
XM_006715479.3:c.188A>C	XP_006715542.1:p.Asn63Thr
NM_001164694.2:c.353A>C	NP_001158166.1:p.Asn118Thr
NM_001164695.2:c.353A>C	NP_001158167.1:p.Asn118Thr
NM_001318495.2:c.124+51A>C	NP_001305424.1:n.124+51A>C
NM_203395.3:c.353A>C MANE Select	NP_981932.1:p.Asn118Thr
NR_134655.2:n.373A>C