Canonical Allele Identifier: CA2435957595

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.69957124G= , CM000685.2:g.69957124G=	GRCh38
NC_000023.10:g.69176974G= , CM000685.1:g.69176974G=	GRCh37
NC_000023.9:g.69093699G=	NCBI36
NG_009809.1:g.346064G=
NG_009809.2:g.346058G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.494G= MANE Select	ENSP00000363680.4:p.Gly165=
ENST00000374548.5:n.736G=
ENST00000374552.8:c.494G=	ENSP00000363680.4:p.Gly165=
ENST00000374553.6:c.494G=	ENSP00000363681.2:p.Gly165=
ENST00000502251.5:n.787G=
ENST00000503592.5:c.98G=	ENSP00000423037.1:p.Gly33=
ENST00000524573.5:c.494G=	ENSP00000432585.1:p.Gly165=
ENST00000533317.5:n.1109G=
ENST00000616899.1:c.98G=	ENSP00000481963.1:p.Gly33=
NM_001005609.1:c.494G=	NP_001005609.1:p.Gly165=
NM_001005612.2:c.494G=	NP_001005612.2:p.Gly165=
NM_001399.4:c.494G=	NP_001390.1:p.Gly165=
XM_006724630.2:c.494G=	XP_006724693.1:p.Gly165=
XM_011530885.1:c.494G=	XP_011529187.1:p.Gly165=
XM_011530885.2:c.494G=	XP_011529187.1:p.Gly165=
XM_017029336.1:c.494G=	XP_016884825.1:p.Gly165=
NM_001399.5:c.494G= MANE Select	NP_001390.1:p.Gly165=
NM_001005609.2:c.494G=	NP_001005609.1:p.Gly165=
NM_001005612.3:c.494G=	NP_001005612.2:p.Gly165=