Canonical Allele Identifier: CA366030308

Gene: IYD

Linked Data

• MyVariant Identifiers: chr6:g.150710580C>A (hg19) ; chr6:g.150389444C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389444C>A , CM000668.2:g.150389444C>A	GRCh38
NC_000006.11:g.150710580C>A , CM000668.1:g.150710580C>A	GRCh37
NC_000006.10:g.150752273C>A	NCBI36
NG_016007.1:g.25553C>A
NG_016007.2:g.25553C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344419.8:c.271C>A MANE Select	ENSP00000343763.4:p.Gln91Lys
ENST00000229447.9:c.271C>A	ENSP00000229447.5:p.Gln91Lys
ENST00000344419.7:c.271C>A	ENSP00000343763.3:p.Gln91Lys
ENST00000367335.7:c.271C>A	ENSP00000356304.3:p.Gln91Lys
ENST00000392255.7:c.271C>A	ENSP00000376084.3:p.Gln91Lys
ENST00000392256.6:c.271C>A	ENSP00000376085.2:p.Gln91Lys
ENST00000422583.2:c.148C>A	ENSP00000397342.2:p.Gln50Lys
ENST00000425615.3:c.106C>A	ENSP00000390081.3:p.Gln36Lys
ENST00000500320.7:c.271C>A	ENSP00000441276.1:p.Gln91Lys
ENST00000546121.1:n.214C>A
NM_001164694.1:c.271C>A	NP_001158166.1:p.Gln91Lys
NM_001164695.1:c.271C>A	NP_001158167.1:p.Gln91Lys
NM_203395.2:c.271C>A	NP_981932.1:p.Gln91Lys
XM_006715478.2:c.271C>A	XP_006715541.1:p.Gln91Lys
XM_006715479.2:c.106C>A	XP_006715542.1:p.Gln36Lys
XR_245516.3:n.434C>A
NM_001318495.1:c.93C>A	NP_001305424.1:p.Leu31=
NR_134655.1:n.411C>A
XM_006715478.3:c.271C>A	XP_006715541.1:p.Gln91Lys
XM_006715479.3:c.106C>A	XP_006715542.1:p.Gln36Lys
NM_001164694.2:c.271C>A	NP_001158166.1:p.Gln91Lys
NM_001164695.2:c.271C>A	NP_001158167.1:p.Gln91Lys
NM_001318495.2:c.93C>A	NP_001305424.1:p.Leu31=
NM_203395.3:c.271C>A MANE Select	NP_981932.1:p.Gln91Lys
NR_134655.2:n.291C>A