Canonical Allele Identifier: CA2578769999

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389612A>C , CM000668.2:g.150389612A>C	GRCh38
NC_000006.11:g.150710748A>C , CM000668.1:g.150710748A>C	GRCh37
NC_000006.10:g.150752441A>C	NCBI36
NG_016007.1:g.25721A>C
NG_016007.2:g.25721A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.370+69A>C MANE Select	ENSP00000343763.4:n.370+69A>C
ENST00000229447.9:c.370+69A>C	ENSP00000229447.5:n.370+69A>C
ENST00000344419.7:c.370+69A>C	ENSP00000343763.3:n.370+69A>C
ENST00000367335.7:c.370+69A>C	ENSP00000356304.3:n.370+69A>C
ENST00000392255.7:c.370+69A>C	ENSP00000376084.3:n.370+69A>C
ENST00000392256.6:c.370+69A>C	ENSP00000376085.2:n.370+69A>C
ENST00000422583.2:c.179+137A>C	ENSP00000397342.2:n.179+137A>C
ENST00000425615.3:c.205+69A>C	ENSP00000390081.3:n.205+69A>C
ENST00000500320.7:c.370+69A>C	ENSP00000441276.1:n.370+69A>C
ENST00000546121.1:n.382A>C
NM_001164694.1:c.370+69A>C	NP_001158166.1:n.370+69A>C
NM_001164695.1:c.370+69A>C	NP_001158167.1:n.370+69A>C
NM_203395.2:c.370+69A>C	NP_981932.1:n.370+69A>C
XM_006715478.2:c.370+69A>C	XP_006715541.1:n.370+69A>C
XM_006715479.2:c.205+69A>C	XP_006715542.1:n.205+69A>C
XR_245516.3:n.533+69A>C
NM_001318495.1:c.124+137A>C	NP_001305424.1:n.124+137A>C
NR_134655.1:n.510+69A>C
XM_006715478.3:c.370+69A>C	XP_006715541.1:n.370+69A>C
XM_006715479.3:c.205+69A>C	XP_006715542.1:n.205+69A>C
NM_001164694.2:c.370+69A>C	NP_001158166.1:n.370+69A>C
NM_001164695.2:c.370+69A>C	NP_001158167.1:n.370+69A>C
NM_001318495.2:c.124+137A>C	NP_001305424.1:n.124+137A>C
NM_203395.3:c.370+69A>C MANE Select	NP_981932.1:n.370+69A>C
NR_134655.2:n.390+69A>C