Canonical Allele Identifier: CA1672406206
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399042_150399043delinsCA , CM000668.2:g.150399042_150399043delinsCA GRCh38
NC_000006.11:g.150720178_150720179delinsCA , CM000668.1:g.150720178_150720179delinsCA GRCh37
NC_000006.10:g.150761871_150761872delinsCA NCBI36
NG_016007.1:g.35151_35152delinsCA
NG_016007.2:g.35151_35152delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*805_*806delinsCA MANE Select ENSP00000343763.4:n.*805_*806delinsCA
ENST00000229447.9:c.*905_*906delinsCA ENSP00000229447.5:n.*905_*906delinsCA
ENST00000344419.7:c.*805_*806delinsCA ENSP00000343763.3:n.*805_*806delinsCA
NM_001164694.1:c.*905_*906delinsCA NP_001158166.1:n.*905_*906delinsCA
NM_001164695.1:c.*992_*993delinsCA NP_001158167.1:n.*992_*993delinsCA
NM_203395.2:c.*805_*806delinsCA NP_981932.1:n.*805_*806delinsCA
NM_001318495.1:c.*805_*806delinsCA NP_001305424.1:n.*805_*806delinsCA
NR_134655.1:n.1988_1989delinsCA
NM_001164694.2:c.*905_*906delinsCA NP_001158166.1:n.*905_*906delinsCA
NM_001164695.2:c.*992_*993delinsCA NP_001158167.1:n.*992_*993delinsCA
NM_001318495.2:c.*805_*806delinsCA NP_001305424.1:n.*805_*806delinsCA
NM_203395.3:c.*805_*806delinsCA MANE Select NP_981932.1:n.*805_*806delinsCA
NR_134655.2:n.1868_1869delinsCA