Canonical Allele Identifier: CA2435979573

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027924_70027925delinsAC , CM000685.2:g.70027924_70027925delinsAC	GRCh38
NC_000023.10:g.69247774_69247775delinsAC , CM000685.1:g.69247774_69247775delinsAC	GRCh37
NC_000023.9:g.69164499_69164500delinsAC	NCBI36
NG_009809.1:g.416864_416865delinsAC
NG_009809.2:g.416858_416859delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.594_595delinsAC MANE Select	ENSP00000363680.4:p.Gly198=
ENST00000374552.8:c.594_595delinsAC	ENSP00000363680.4:p.Gly198=
ENST00000374553.6:c.594_595delinsAC	ENSP00000363681.2:p.Gly198=
ENST00000503592.5:c.198_199delinsAC	ENSP00000423037.1:p.Gly66=
ENST00000524573.5:c.594_595delinsAC	ENSP00000432585.1:p.Gly198=
ENST00000616899.1:c.198_199delinsAC	ENSP00000481963.1:p.Gly66=
NM_001005609.1:c.594_595delinsAC	NP_001005609.1:p.Gly198=
NM_001005612.2:c.594_595delinsAC	NP_001005612.2:p.Gly198=
NM_001399.4:c.594_595delinsAC	NP_001390.1:p.Gly198=
XM_006724630.2:c.594_595delinsAC	XP_006724693.1:p.Gly198=
XM_011530885.1:c.594_595delinsAC	XP_011529187.1:p.Gly198=
XM_011530885.2:c.594_595delinsAC	XP_011529187.1:p.Gly198=
XM_017029336.1:c.594_595delinsAC	XP_016884825.1:p.Gly198=
NM_001399.5:c.594_595delinsAC MANE Select	NP_001390.1:p.Gly198=
NM_001005609.2:c.594_595delinsAC	NP_001005609.1:p.Gly198=
NM_001005612.3:c.594_595delinsAC	NP_001005612.2:p.Gly198=