Canonical Allele Identifier: CA2435981320

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033499G= , CM000685.2:g.70033499G=	GRCh38
NC_000023.10:g.69253349G= , CM000685.1:g.69253349G=	GRCh37
NC_000023.9:g.69170074G=	NCBI36
NG_009809.1:g.422439G=
NG_009809.2:g.422433G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001399.5:c.895G= MANE Select	NP_001390.1:p.Gly299=
ENST00000374552.9:c.895G= MANE Select	ENSP00000363680.4:p.Gly299=
NM_001005609.1:c.895G=	NP_001005609.1:p.Gly299=
NM_001005609.2:c.895G=	NP_001005609.1:p.Gly299=
NM_001005612.2:c.886G=	NP_001005612.2:p.Gly296=
NM_001005612.3:c.886G=	NP_001005612.2:p.Gly296=
NM_001399.4:c.895G=	NP_001390.1:p.Gly299=
ENST00000374552.8:c.895G=	ENSP00000363680.4:p.Gly299=
ENST00000374553.6:c.895G=	ENSP00000363681.2:p.Gly299=
ENST00000524573.5:c.886G=	ENSP00000432585.1:p.Gly296=
ENST00000616899.1:c.499G=	ENSP00000481963.1:p.Gly167=
XM_006724630.2:c.886G=	XP_006724693.1:p.Gly296=
XM_011530885.1:c.895G=	XP_011529187.1:p.Gly299=
XM_011530885.2:c.895G=	XP_011529187.1:p.Gly299=
XM_017029336.1:c.882+13G=	XP_016884825.1:n.882+13G=