Canonical Allele Identifier: CA2821678336

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027819T>A , CM000685.2:g.70027819T>A	GRCh38
NC_000023.10:g.69247669T>A , CM000685.1:g.69247669T>A	GRCh37
NC_000023.9:g.69164394T>A	NCBI36
NG_009809.1:g.416759T>A
NG_009809.2:g.416753T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.527-38T>A MANE Select	ENSP00000363680.4:n.527-38T>A
ENST00000374552.8:c.527-38T>A	ENSP00000363680.4:n.527-38T>A
ENST00000374553.6:c.527-38T>A	ENSP00000363681.2:n.527-38T>A
ENST00000503592.5:c.131-38T>A	ENSP00000423037.1:n.131-38T>A
ENST00000524573.5:c.527-38T>A	ENSP00000432585.1:n.527-38T>A
ENST00000616899.1:c.131-38T>A	ENSP00000481963.1:n.131-38T>A
NM_001005609.1:c.527-38T>A	NP_001005609.1:n.527-38T>A
NM_001005612.2:c.527-38T>A	NP_001005612.2:n.527-38T>A
NM_001399.4:c.527-38T>A	NP_001390.1:n.527-38T>A
XM_006724630.2:c.527-38T>A	XP_006724693.1:n.527-38T>A
XM_011530885.1:c.527-38T>A	XP_011529187.1:n.527-38T>A
XM_011530885.2:c.527-38T>A	XP_011529187.1:n.527-38T>A
XM_017029336.1:c.527-38T>A	XP_016884825.1:n.527-38T>A
NM_001399.5:c.527-38T>A MANE Select	NP_001390.1:n.527-38T>A
NM_001005609.2:c.527-38T>A	NP_001005609.1:n.527-38T>A
NM_001005612.3:c.527-38T>A	NP_001005612.2:n.527-38T>A