Canonical Allele Identifier: CA2821678337

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027930_70027947del , CM000685.2:g.70027930_70027947del	GRCh38
NC_000023.10:g.69247780_69247797del , CM000685.1:g.69247780_69247797del	GRCh37
NC_000023.9:g.69164505_69164522del	NCBI36
NG_009809.1:g.416870_416887del
NG_009809.2:g.416864_416881del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.600_617del MANE Select	ENSP00000363680.4:p.Gly201_Pro206del
ENST00000374552.8:c.600_617del	ENSP00000363680.4:p.Gly201_Pro206del
ENST00000374553.6:c.600_617del	ENSP00000363681.2:p.Gly201_Pro206del
ENST00000503592.5:c.204_221del	ENSP00000423037.1:p.Gly69_Pro74del
ENST00000524573.5:c.600_617del	ENSP00000432585.1:p.Gly201_Pro206del
ENST00000616899.1:c.204_221del	ENSP00000481963.1:p.Gly69_Pro74del
NM_001005609.1:c.600_617del	NP_001005609.1:p.Gly201_Pro206del
NM_001005612.2:c.600_617del	NP_001005612.2:p.Gly201_Pro206del
NM_001399.4:c.600_617del	NP_001390.1:p.Gly201_Pro206del
XM_006724630.2:c.600_617del	XP_006724693.1:p.Gly201_Pro206del
XM_011530885.1:c.600_617del	XP_011529187.1:p.Gly201_Pro206del
XM_011530885.2:c.600_617del	XP_011529187.1:p.Gly201_Pro206del
XM_017029336.1:c.600_617del	XP_016884825.1:p.Gly201_Pro206del
NM_001399.5:c.600_617del MANE Select	NP_001390.1:p.Gly201_Pro206del
NM_001005609.2:c.600_617del	NP_001005609.1:p.Gly201_Pro206del
NM_001005612.3:c.600_617del	NP_001005612.2:p.Gly201_Pro206del