Canonical Allele Identifier: CA517013951

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69253288T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033438T>A , CM000685.2:g.70033438T>A	GRCh38
NC_000023.10:g.69253288T>A , CM000685.1:g.69253288T>A	GRCh37
NC_000023.9:g.69170013T>A	NCBI36
NG_009809.1:g.422378T>A
NG_009809.2:g.422372T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.834T>A MANE Select	ENSP00000363680.4:p.Thr278=
ENST00000374552.8:c.834T>A	ENSP00000363680.4:p.Thr278=
ENST00000374553.6:c.834T>A	ENSP00000363681.2:p.Thr278=
ENST00000524573.5:c.825T>A	ENSP00000432585.1:p.Thr275=
ENST00000616899.1:c.438T>A	ENSP00000481963.1:p.Thr146=
NM_001005609.1:c.834T>A	NP_001005609.1:p.Thr278=
NM_001005612.2:c.825T>A	NP_001005612.2:p.Thr275=
NM_001399.4:c.834T>A	NP_001390.1:p.Thr278=
XM_006724630.2:c.825T>A	XP_006724693.1:p.Thr275=
XM_011530885.1:c.834T>A	XP_011529187.1:p.Thr278=
XM_011530885.2:c.834T>A	XP_011529187.1:p.Thr278=
XM_017029336.1:c.834T>A	XP_016884825.1:p.Thr278=
NM_001399.5:c.834T>A MANE Select	NP_001390.1:p.Thr278=
NM_001005609.2:c.834T>A	NP_001005609.1:p.Thr278=
NM_001005612.3:c.825T>A	NP_001005612.2:p.Thr275=