Canonical Allele Identifier: CA2568923434

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033591T>G , CM000685.2:g.70033591T>G	GRCh38
NC_000023.10:g.69253441T>G , CM000685.1:g.69253441T>G	GRCh37
NC_000023.9:g.69170166T>G	NCBI36
NG_009809.1:g.422531T>G
NG_009809.2:g.422525T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.924+63T>G MANE Select	ENSP00000363680.4:n.924+63T>G
ENST00000374552.8:c.924+63T>G	ENSP00000363680.4:n.924+63T>G
ENST00000374553.6:c.918+69T>G	ENSP00000363681.2:n.918+69T>G
ENST00000524573.5:c.909+69T>G	ENSP00000432585.1:n.909+69T>G
ENST00000616899.1:c.528+63T>G	ENSP00000481963.1:n.528+63T>G
NM_001005609.1:c.918+69T>G	NP_001005609.1:n.918+69T>G
NM_001005612.2:c.909+69T>G	NP_001005612.2:n.909+69T>G
NM_001399.4:c.924+63T>G	NP_001390.1:n.924+63T>G
XM_006724630.2:c.915+63T>G	XP_006724693.1:n.915+63T>G
XM_011530885.1:c.918+69T>G	XP_011529187.1:n.918+69T>G
XM_011530885.2:c.918+69T>G	XP_011529187.1:n.918+69T>G
XM_017029336.1:c.882+105T>G	XP_016884825.1:n.882+105T>G
NM_001399.5:c.924+63T>G MANE Select	NP_001390.1:n.924+63T>G
NM_001005609.2:c.918+69T>G	NP_001005609.1:n.918+69T>G
NM_001005612.3:c.909+69T>G	NP_001005612.2:n.909+69T>G