Canonical Allele Identifier: CA1672406223
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399088A= , CM000668.2:g.150399088A= GRCh38
NC_000006.11:g.150720224A= , CM000668.1:g.150720224A= GRCh37
NC_000006.10:g.150761917A= NCBI36
NG_016007.1:g.35197A=
NG_016007.2:g.35197A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*851A= MANE Select ENSP00000343763.4:n.*851A=
ENST00000229447.9:c.*951A= ENSP00000229447.5:n.*951A=
ENST00000344419.7:c.*851A= ENSP00000343763.3:n.*851A=
NM_001164694.1:c.*951A= NP_001158166.1:n.*951A=
NM_001164695.1:c.*1038A= NP_001158167.1:n.*1038A=
NM_203395.2:c.*851A= NP_981932.1:n.*851A=
NM_001318495.1:c.*851A= NP_001305424.1:n.*851A=
NR_134655.1:n.2034A=
NM_001164694.2:c.*951A= NP_001158166.1:n.*951A=
NM_001164695.2:c.*1038A= NP_001158167.1:n.*1038A=
NM_001318495.2:c.*851A= NP_001305424.1:n.*851A=
NM_203395.3:c.*851A= MANE Select NP_981932.1:n.*851A=
NR_134655.2:n.1914A=