Canonical Allele Identifier: CA2435979443

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027668C= , CM000685.2:g.70027668C=	GRCh38
NC_000023.10:g.69247518C= , CM000685.1:g.69247518C=	GRCh37
NC_000023.9:g.69164243C=	NCBI36
NG_009809.1:g.416608C=
NG_009809.2:g.416602C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.527-189C= MANE Select	ENSP00000363680.4:n.527-189C=
ENST00000374552.8:c.527-189C=	ENSP00000363680.4:n.527-189C=
ENST00000374553.6:c.527-189C=	ENSP00000363681.2:n.527-189C=
ENST00000503592.5:c.131-189C=	ENSP00000423037.1:n.131-189C=
ENST00000524573.5:c.527-189C=	ENSP00000432585.1:n.527-189C=
ENST00000616899.1:c.131-189C=	ENSP00000481963.1:n.131-189C=
NM_001005609.1:c.527-189C=	NP_001005609.1:n.527-189C=
NM_001005612.2:c.527-189C=	NP_001005612.2:n.527-189C=
NM_001399.4:c.527-189C=	NP_001390.1:n.527-189C=
XM_006724630.2:c.527-189C=	XP_006724693.1:n.527-189C=
XM_011530885.1:c.527-189C=	XP_011529187.1:n.527-189C=
XM_011530885.2:c.527-189C=	XP_011529187.1:n.527-189C=
XM_017029336.1:c.527-189C=	XP_016884825.1:n.527-189C=
NM_001399.5:c.527-189C= MANE Select	NP_001390.1:n.527-189C=
NM_001005609.2:c.527-189C=	NP_001005609.1:n.527-189C=
NM_001005612.3:c.527-189C=	NP_001005612.2:n.527-189C=