Canonical Allele Identifier: CA2435979566

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027915_70027916delinsAC , CM000685.2:g.70027915_70027916delinsAC	GRCh38
NC_000023.10:g.69247765_69247766delinsAC , CM000685.1:g.69247765_69247766delinsAC	GRCh37
NC_000023.9:g.69164490_69164491delinsAC	NCBI36
NG_009809.1:g.416855_416856delinsAC
NG_009809.2:g.416849_416850delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.585_586delinsAC MANE Select	ENSP00000363680.4:p.Gly195=
ENST00000374552.8:c.585_586delinsAC	ENSP00000363680.4:p.Gly195=
ENST00000374553.6:c.585_586delinsAC	ENSP00000363681.2:p.Gly195=
ENST00000503592.5:c.189_190delinsAC	ENSP00000423037.1:p.Gly63=
ENST00000524573.5:c.585_586delinsAC	ENSP00000432585.1:p.Gly195=
ENST00000616899.1:c.189_190delinsAC	ENSP00000481963.1:p.Gly63=
NM_001005609.1:c.585_586delinsAC	NP_001005609.1:p.Gly195=
NM_001005612.2:c.585_586delinsAC	NP_001005612.2:p.Gly195=
NM_001399.4:c.585_586delinsAC	NP_001390.1:p.Gly195=
XM_006724630.2:c.585_586delinsAC	XP_006724693.1:p.Gly195=
XM_011530885.1:c.585_586delinsAC	XP_011529187.1:p.Gly195=
XM_011530885.2:c.585_586delinsAC	XP_011529187.1:p.Gly195=
XM_017029336.1:c.585_586delinsAC	XP_016884825.1:p.Gly195=
NM_001399.5:c.585_586delinsAC MANE Select	NP_001390.1:p.Gly195=
NM_001005609.2:c.585_586delinsAC	NP_001005609.1:p.Gly195=
NM_001005612.3:c.585_586delinsAC	NP_001005612.2:p.Gly195=