Canonical Allele Identifier: CA2740053698

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.69957151T>A , CM000685.2:g.69957151T>A	GRCh38
NC_000023.10:g.69177001T>A , CM000685.1:g.69177001T>A	GRCh37
NC_000023.9:g.69093726T>A	NCBI36
NG_009809.1:g.346091T>A
NG_009809.2:g.346085T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.502+19T>A MANE Select	ENSP00000363680.4:n.502+19T>A
ENST00000374548.5:n.763T>A
ENST00000374552.8:c.502+19T>A	ENSP00000363680.4:n.502+19T>A
ENST00000374553.6:c.502+19T>A	ENSP00000363681.2:n.502+19T>A
ENST00000502251.5:n.814T>A
ENST00000503592.5:c.106+19T>A	ENSP00000423037.1:n.106+19T>A
ENST00000524573.5:c.502+19T>A	ENSP00000432585.1:n.502+19T>A
ENST00000533317.5:n.1136T>A
ENST00000616899.1:c.106+19T>A	ENSP00000481963.1:n.106+19T>A
NM_001005609.1:c.502+19T>A	NP_001005609.1:n.502+19T>A
NM_001005612.2:c.502+19T>A	NP_001005612.2:n.502+19T>A
NM_001399.4:c.502+19T>A	NP_001390.1:n.502+19T>A
XM_006724630.2:c.502+19T>A	XP_006724693.1:n.502+19T>A
XM_011530885.1:c.502+19T>A	XP_011529187.1:n.502+19T>A
XM_011530885.2:c.502+19T>A	XP_011529187.1:n.502+19T>A
XM_017029336.1:c.502+19T>A	XP_016884825.1:n.502+19T>A
NM_001399.5:c.502+19T>A MANE Select	NP_001390.1:n.502+19T>A
NM_001005609.2:c.502+19T>A	NP_001005609.1:n.502+19T>A
NM_001005612.3:c.502+19T>A	NP_001005612.2:n.502+19T>A