Canonical Allele Identifier: CA366029659

Gene: IYD

Linked Data

• gnomAD v4: 6-150389355-C-T
• COSMIC: COSM4693687 ; COSM4693688 ; COSM4693689 ; COSM4693690
• MyVariant Identifiers: chr6:g.150710491C>T (hg19) ; chr6:g.150389355C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389355C>T , CM000668.2:g.150389355C>T	GRCh38
NC_000006.11:g.150710491C>T , CM000668.1:g.150710491C>T	GRCh37
NC_000006.10:g.150752184C>T	NCBI36
NG_016007.1:g.25464C>T
NG_016007.2:g.25464C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.182C>T MANE Select	ENSP00000343763.4:p.Ala61Val
ENST00000229447.9:c.182C>T	ENSP00000229447.5:p.Ala61Val
ENST00000344419.7:c.182C>T	ENSP00000343763.3:p.Ala61Val
ENST00000367335.7:c.182C>T	ENSP00000356304.3:p.Ala61Val
ENST00000392255.7:c.182C>T	ENSP00000376084.3:p.Ala61Val
ENST00000392256.6:c.182C>T	ENSP00000376085.2:p.Ala61Val
ENST00000422583.2:c.59C>T	ENSP00000397342.2:p.Ala20Val
ENST00000425615.3:c.17C>T	ENSP00000390081.3:p.Ala6Val
ENST00000500320.7:c.182C>T	ENSP00000441276.1:p.Ala61Val
ENST00000546121.1:n.125C>T
NM_001164694.1:c.182C>T	NP_001158166.1:p.Ala61Val
NM_001164695.1:c.182C>T	NP_001158167.1:p.Ala61Val
NM_203395.2:c.182C>T	NP_981932.1:p.Ala61Val
XM_006715478.2:c.182C>T	XP_006715541.1:p.Ala61Val
XM_006715479.2:c.17C>T	XP_006715542.1:p.Ala6Val
XR_245516.3:n.345C>T
NM_001318495.1:c.4C>T	NP_001305424.1:p.Leu2=
NR_134655.1:n.322C>T
XM_006715478.3:c.182C>T	XP_006715541.1:p.Ala61Val
XM_006715479.3:c.17C>T	XP_006715542.1:p.Ala6Val
NM_001164694.2:c.182C>T	NP_001158166.1:p.Ala61Val
NM_001164695.2:c.182C>T	NP_001158167.1:p.Ala61Val
NM_001318495.2:c.4C>T	NP_001305424.1:p.Leu2=
NM_203395.3:c.182C>T MANE Select	NP_981932.1:p.Ala61Val
NR_134655.2:n.202C>T