Canonical Allele Identifier: CA2435981909

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035394G= , CM000685.2:g.70035394G=	GRCh38
NC_000023.10:g.69255244G= , CM000685.1:g.69255244G=	GRCh37
NC_000023.9:g.69171969G=	NCBI36
NG_009809.1:g.424334G=
NG_009809.2:g.424328G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001399.5:c.961G= MANE Select	NP_001390.1:p.Glu321=
ENST00000374552.9:c.961G= MANE Select	ENSP00000363680.4:p.Glu321=
NM_001005609.1:c.955G=	NP_001005609.1:p.Glu319=
NM_001005609.2:c.955G=	NP_001005609.1:p.Glu319=
NM_001005612.2:c.946G=	NP_001005612.2:p.Glu316=
NM_001005612.3:c.946G=	NP_001005612.2:p.Glu316=
NM_001399.4:c.961G=	NP_001390.1:p.Glu321=
ENST00000374552.8:c.961G=	ENSP00000363680.4:p.Glu321=
ENST00000374553.6:c.955G=	ENSP00000363681.2:p.Glu319=
ENST00000524573.5:c.946G=	ENSP00000432585.1:p.Glu316=
ENST00000616899.1:c.565G=	ENSP00000481963.1:p.Glu189=
XM_006724630.2:c.952G=	XP_006724693.1:p.Glu318=
XM_017029336.1:c.919G=	XP_016884825.1:p.Glu307=