Canonical Allele Identifier: CA1672406181

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399003A= , CM000668.2:g.150399003A=	GRCh38
NC_000006.11:g.150720139A= , CM000668.1:g.150720139A=	GRCh37
NC_000006.10:g.150761832A=	NCBI36
NG_016007.1:g.35112A=
NG_016007.2:g.35112A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*766A= MANE Select	ENSP00000343763.4:n.*766A=
ENST00000229447.9:c.*866A=	ENSP00000229447.5:n.*866A=
ENST00000344419.7:c.*766A=	ENSP00000343763.3:n.*766A=
NM_001164694.1:c.*866A=	NP_001158166.1:n.*866A=
NM_001164695.1:c.*953A=	NP_001158167.1:n.*953A=
NM_203395.2:c.*766A=	NP_981932.1:n.*766A=
NM_001318495.1:c.*766A=	NP_001305424.1:n.*766A=
NR_134655.1:n.1949A=
NM_001164694.2:c.*866A=	NP_001158166.1:n.*866A=
NM_001164695.2:c.*953A=	NP_001158167.1:n.*953A=
NM_001318495.2:c.*766A=	NP_001305424.1:n.*766A=
NM_203395.3:c.*766A= MANE Select	NP_981932.1:n.*766A=
NR_134655.2:n.1829A=