Canonical Allele Identifier: CA2680762418

Gene: IYD

Linked Data

• gnomAD v4: 6-150398678-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398678G>T , CM000668.2:g.150398678G>T	GRCh38
NC_000006.11:g.150719814G>T , CM000668.1:g.150719814G>T	GRCh37
NC_000006.10:g.150761507G>T	NCBI36
NG_016007.1:g.34787G>T
NG_016007.2:g.34787G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*441G>T MANE Select	ENSP00000343763.4:n.*441G>T
ENST00000229447.9:c.*541G>T	ENSP00000229447.5:n.*541G>T
ENST00000344419.7:c.*441G>T	ENSP00000343763.3:n.*441G>T
NM_001164694.1:c.*541G>T	NP_001158166.1:n.*541G>T
NM_001164695.1:c.*628G>T	NP_001158167.1:n.*628G>T
NM_203395.2:c.*441G>T	NP_981932.1:n.*441G>T
NM_001318495.1:c.*441G>T	NP_001305424.1:n.*441G>T
NR_134655.1:n.1624G>T
NM_001164694.2:c.*541G>T	NP_001158166.1:n.*541G>T
NM_001164695.2:c.*628G>T	NP_001158167.1:n.*628G>T
NM_001318495.2:c.*441G>T	NP_001305424.1:n.*441G>T
NM_203395.3:c.*441G>T MANE Select	NP_981932.1:n.*441G>T
NR_134655.2:n.1504G>T