Canonical Allele Identifier: CA366030728

Gene: IYD

Linked Data

• MyVariant Identifiers: chr6:g.150710643C>A (hg19) ; chr6:g.150389507C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389507C>A , CM000668.2:g.150389507C>A	GRCh38
NC_000006.11:g.150710643C>A , CM000668.1:g.150710643C>A	GRCh37
NC_000006.10:g.150752336C>A	NCBI36
NG_016007.1:g.25616C>A
NG_016007.2:g.25616C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.334C>A MANE Select	ENSP00000343763.4:p.Pro112Thr
ENST00000229447.9:c.334C>A	ENSP00000229447.5:p.Pro112Thr
ENST00000344419.7:c.334C>A	ENSP00000343763.3:p.Pro112Thr
ENST00000367335.7:c.334C>A	ENSP00000356304.3:p.Pro112Thr
ENST00000392255.7:c.334C>A	ENSP00000376084.3:p.Pro112Thr
ENST00000392256.6:c.334C>A	ENSP00000376085.2:p.Pro112Thr
ENST00000422583.2:c.179+32C>A	ENSP00000397342.2:n.179+32C>A
ENST00000425615.3:c.169C>A	ENSP00000390081.3:p.Pro57Thr
ENST00000500320.7:c.334C>A	ENSP00000441276.1:p.Pro112Thr
ENST00000546121.1:n.277C>A
NM_001164694.1:c.334C>A	NP_001158166.1:p.Pro112Thr
NM_001164695.1:c.334C>A	NP_001158167.1:p.Pro112Thr
NM_203395.2:c.334C>A	NP_981932.1:p.Pro112Thr
XM_006715478.2:c.334C>A	XP_006715541.1:p.Pro112Thr
XM_006715479.2:c.169C>A	XP_006715542.1:p.Pro57Thr
XR_245516.3:n.497C>A
NM_001318495.1:c.124+32C>A	NP_001305424.1:n.124+32C>A
NR_134655.1:n.474C>A
XM_006715478.3:c.334C>A	XP_006715541.1:p.Pro112Thr
XM_006715479.3:c.169C>A	XP_006715542.1:p.Pro57Thr
NM_001164694.2:c.334C>A	NP_001158166.1:p.Pro112Thr
NM_001164695.2:c.334C>A	NP_001158167.1:p.Pro112Thr
NM_001318495.2:c.124+32C>A	NP_001305424.1:n.124+32C>A
NM_203395.3:c.334C>A MANE Select	NP_981932.1:p.Pro112Thr
NR_134655.2:n.354C>A