Canonical Allele Identifier: CA366029643

Gene: IYD

Linked Data

• MyVariant Identifiers: chr6:g.150710487G>C (hg19) ; chr6:g.150389351G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389351G>C , CM000668.2:g.150389351G>C	GRCh38
NC_000006.11:g.150710487G>C , CM000668.1:g.150710487G>C	GRCh37
NC_000006.10:g.150752180G>C	NCBI36
NG_016007.1:g.25460G>C
NG_016007.2:g.25460G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344419.8:c.179-1G>C MANE Select	ENSP00000343763.4:n.179-1G>C
ENST00000229447.9:c.179-1G>C	ENSP00000229447.5:n.179-1G>C
ENST00000344419.7:c.179-1G>C	ENSP00000343763.3:n.179-1G>C
ENST00000367335.7:c.179-1G>C	ENSP00000356304.3:n.179-1G>C
ENST00000392255.7:c.179-1G>C	ENSP00000376084.3:n.179-1G>C
ENST00000392256.6:c.179-1G>C	ENSP00000376085.2:n.179-1G>C
ENST00000422583.2:c.56-1G>C	ENSP00000397342.2:n.56-1G>C
ENST00000425615.3:c.14-1G>C	ENSP00000390081.3:n.14-1G>C
ENST00000500320.7:c.179-1G>C	ENSP00000441276.1:n.179-1G>C
ENST00000546121.1:n.122-1G>C
NM_001164694.1:c.179-1G>C	NP_001158166.1:n.179-1G>C
NM_001164695.1:c.179-1G>C	NP_001158167.1:n.179-1G>C
NM_203395.2:c.179-1G>C	NP_981932.1:n.179-1G>C
XM_006715478.2:c.179-1G>C	XP_006715541.1:n.179-1G>C
XM_006715479.2:c.14-1G>C	XP_006715542.1:n.14-1G>C
XR_245516.3:n.342-1G>C
NM_001318495.1:c.1-1G>C	NP_001305424.1:n.1-1G>C
NR_134655.1:n.319-1G>C
XM_006715478.3:c.179-1G>C	XP_006715541.1:n.179-1G>C
XM_006715479.3:c.14-1G>C	XP_006715542.1:n.14-1G>C
NM_001164694.2:c.179-1G>C	NP_001158166.1:n.179-1G>C
NM_001164695.2:c.179-1G>C	NP_001158167.1:n.179-1G>C
NM_001318495.2:c.1-1G>C	NP_001305424.1:n.1-1G>C
NM_203395.3:c.179-1G>C MANE Select	NP_981932.1:n.179-1G>C
NR_134655.2:n.199-1G>C