Canonical Allele Identifier: CA2773539391

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398645_150398646insCTG , CM000668.2:g.150398645_150398646insCTG	GRCh38
NC_000006.11:g.150719781_150719782insCTG , CM000668.1:g.150719781_150719782insCTG	GRCh37
NC_000006.10:g.150761474_150761475insCTG	NCBI36
NG_016007.1:g.34754_34755insCTG
NG_016007.2:g.34754_34755insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*408_*409insCTG MANE Select	ENSP00000343763.4:n.*408_*409insCTG
ENST00000229447.9:c.*508_*509insCTG	ENSP00000229447.5:n.*508_*509insCTG
ENST00000344419.7:c.*408_*409insCTG	ENSP00000343763.3:n.*408_*409insCTG
NM_001164694.1:c.*508_*509insCTG	NP_001158166.1:n.*508_*509insCTG
NM_001164695.1:c.*595_*596insCTG	NP_001158167.1:n.*595_*596insCTG
NM_203395.2:c.*408_*409insCTG	NP_981932.1:n.*408_*409insCTG
NM_001318495.1:c.*408_*409insCTG	NP_001305424.1:n.*408_*409insCTG
NR_134655.1:n.1591_1592insCTG
NM_001164694.2:c.*508_*509insCTG	NP_001158166.1:n.*508_*509insCTG
NM_001164695.2:c.*595_*596insCTG	NP_001158167.1:n.*595_*596insCTG
NM_001318495.2:c.*408_*409insCTG	NP_001305424.1:n.*408_*409insCTG
NM_203395.3:c.*408_*409insCTG MANE Select	NP_981932.1:n.*408_*409insCTG
NR_134655.2:n.1471_1472insCTG