Canonical Allele Identifier: CA820731627

Gene: IYD

Linked Data

• dbSNP Id: rs1436529734
• MyVariant Identifiers: chr6:g.150720101_150720102insTT (hg19) ; chr6:g.150398965_150398966insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398966_150398967insTT , CM000668.2:g.150398966_150398967insTT	GRCh38
NC_000006.11:g.150720102_150720103insTT , CM000668.1:g.150720102_150720103insTT	GRCh37
NC_000006.10:g.150761795_150761796insTT	NCBI36
NG_016007.1:g.35075_35076insTT
NG_016007.2:g.35075_35076insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*729_*730insTT MANE Select	ENSP00000343763.4:n.*729_*730insTT
ENST00000229447.9:c.*829_*830insTT	ENSP00000229447.5:n.*829_*830insTT
ENST00000344419.7:c.*729_*730insTT	ENSP00000343763.3:n.*729_*730insTT
NM_001164694.1:c.*829_*830insTT	NP_001158166.1:n.*829_*830insTT
NM_001164695.1:c.*916_*917insTT	NP_001158167.1:n.*916_*917insTT
NM_203395.2:c.*729_*730insTT	NP_981932.1:n.*729_*730insTT
NM_001318495.1:c.*729_*730insTT	NP_001305424.1:n.*729_*730insTT
NR_134655.1:n.1912_1913insTT
NM_001164694.2:c.*829_*830insTT	NP_001158166.1:n.*829_*830insTT
NM_001164695.2:c.*916_*917insTT	NP_001158167.1:n.*916_*917insTT
NM_001318495.2:c.*729_*730insTT	NP_001305424.1:n.*729_*730insTT
NM_203395.3:c.*729_*730insTT MANE Select	NP_981932.1:n.*729_*730insTT
NR_134655.2:n.1792_1793insTT