Canonical Allele Identifier: CA2435981927

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035434G= , CM000685.2:g.70035434G=	GRCh38
NC_000023.10:g.69255284G= , CM000685.1:g.69255284G=	GRCh37
NC_000023.9:g.69172009G=	NCBI36
NG_009809.1:g.424374G=
NG_009809.2:g.424368G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.1001G= MANE Select	ENSP00000363680.4:p.Arg334=
ENST00000374552.8:c.1001G=	ENSP00000363680.4:p.Arg334=
ENST00000374553.6:c.995G=	ENSP00000363681.2:p.Arg332=
ENST00000524573.5:c.986G=	ENSP00000432585.1:p.Arg329=
ENST00000616899.1:c.605G=	ENSP00000481963.1:p.Arg202=
NM_001005609.1:c.995G=	NP_001005609.1:p.Arg332=
NM_001005612.2:c.986G=	NP_001005612.2:p.Arg329=
NM_001399.4:c.1001G=	NP_001390.1:p.Arg334=
XM_006724630.2:c.992G=	XP_006724693.1:p.Arg331=
XM_017029336.1:c.959G=	XP_016884825.1:p.Arg320=
NM_001399.5:c.1001G= MANE Select	NP_001390.1:p.Arg334=
NM_001005609.2:c.995G=	NP_001005609.1:p.Arg332=
NM_001005612.3:c.986G=	NP_001005612.2:p.Arg329=