Canonical Allele Identifier: CA1672405992

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398596_150398599delinsCATG , CM000668.2:g.150398596_150398599delinsCATG	GRCh38
NC_000006.11:g.150719732_150719735delinsCATG , CM000668.1:g.150719732_150719735delinsCATG	GRCh37
NC_000006.10:g.150761425_150761428delinsCATG	NCBI36
NG_016007.1:g.34705_34708delinsCATG
NG_016007.2:g.34705_34708delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*359_*362delinsCATG MANE Select	ENSP00000343763.4:n.*359_*362delinsCATG
ENST00000229447.9:c.*459_*462delinsCATG	ENSP00000229447.5:n.*459_*462delinsCATG
ENST00000344419.7:c.*359_*362delinsCATG	ENSP00000343763.3:n.*359_*362delinsCATG
NM_001164694.1:c.*459_*462delinsCATG	NP_001158166.1:n.*459_*462delinsCATG
NM_001164695.1:c.*546_*549delinsCATG	NP_001158167.1:n.*546_*549delinsCATG
NM_203395.2:c.*359_*362delinsCATG	NP_981932.1:n.*359_*362delinsCATG
NM_001318495.1:c.*359_*362delinsCATG	NP_001305424.1:n.*359_*362delinsCATG
NR_134655.1:n.1542_1545delinsCATG
NM_001164694.2:c.*459_*462delinsCATG	NP_001158166.1:n.*459_*462delinsCATG
NM_001164695.2:c.*546_*549delinsCATG	NP_001158167.1:n.*546_*549delinsCATG
NM_001318495.2:c.*359_*362delinsCATG	NP_001305424.1:n.*359_*362delinsCATG
NM_203395.3:c.*359_*362delinsCATG MANE Select	NP_981932.1:n.*359_*362delinsCATG
NR_134655.2:n.1422_1425delinsCATG