Canonical Allele Identifier: CA2435981296

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033434T= , CM000685.2:g.70033434T=	GRCh38
NC_000023.10:g.69253284T= , CM000685.1:g.69253284T=	GRCh37
NC_000023.9:g.69170009T=	NCBI36
NG_009809.1:g.422374T=
NG_009809.2:g.422368T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.830T= MANE Select	ENSP00000363680.4:p.Ile277=
ENST00000374552.8:c.830T=	ENSP00000363680.4:p.Ile277=
ENST00000374553.6:c.830T=	ENSP00000363681.2:p.Ile277=
ENST00000524573.5:c.821T=	ENSP00000432585.1:p.Ile274=
ENST00000616899.1:c.434T=	ENSP00000481963.1:p.Ile145=
NM_001005609.1:c.830T=	NP_001005609.1:p.Ile277=
NM_001005612.2:c.821T=	NP_001005612.2:p.Ile274=
NM_001399.4:c.830T=	NP_001390.1:p.Ile277=
XM_006724630.2:c.821T=	XP_006724693.1:p.Ile274=
XM_011530885.1:c.830T=	XP_011529187.1:p.Ile277=
XM_011530885.2:c.830T=	XP_011529187.1:p.Ile277=
XM_017029336.1:c.830T=	XP_016884825.1:p.Ile277=
NM_001399.5:c.830T= MANE Select	NP_001390.1:p.Ile277=
NM_001005609.2:c.830T=	NP_001005609.1:p.Ile277=
NM_001005612.3:c.821T=	NP_001005612.2:p.Ile274=