Canonical Allele Identifier: CA2435981297

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033437C= , CM000685.2:g.70033437C=	GRCh38
NC_000023.10:g.69253287C= , CM000685.1:g.69253287C=	GRCh37
NC_000023.9:g.69170012C=	NCBI36
NG_009809.1:g.422377C=
NG_009809.2:g.422371C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.833C= MANE Select	ENSP00000363680.4:p.Thr278=
ENST00000374552.8:c.833C=	ENSP00000363680.4:p.Thr278=
ENST00000374553.6:c.833C=	ENSP00000363681.2:p.Thr278=
ENST00000524573.5:c.824C=	ENSP00000432585.1:p.Thr275=
ENST00000616899.1:c.437C=	ENSP00000481963.1:p.Thr146=
NM_001005609.1:c.833C=	NP_001005609.1:p.Thr278=
NM_001005612.2:c.824C=	NP_001005612.2:p.Thr275=
NM_001399.4:c.833C=	NP_001390.1:p.Thr278=
XM_006724630.2:c.824C=	XP_006724693.1:p.Thr275=
XM_011530885.1:c.833C=	XP_011529187.1:p.Thr278=
XM_011530885.2:c.833C=	XP_011529187.1:p.Thr278=
XM_017029336.1:c.833C=	XP_016884825.1:p.Thr278=
NM_001399.5:c.833C= MANE Select	NP_001390.1:p.Thr278=
NM_001005609.2:c.833C=	NP_001005609.1:p.Thr278=
NM_001005612.3:c.824C=	NP_001005612.2:p.Thr275=