Canonical Allele Identifier: CA877772169

Gene: EDA

Linked Data

• dbSNP Id: rs1219886043
• gnomAD v3: X-70027718-G-C
• gnomAD v4: X-70027718-G-C
• MyVariant Identifiers: chrX:g.69247568G>C (hg19) ; chrX:g.70027718G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027718G>C , CM000685.2:g.70027718G>C	GRCh38
NC_000023.10:g.69247568G>C , CM000685.1:g.69247568G>C	GRCh37
NC_000023.9:g.69164293G>C	NCBI36
NG_009809.1:g.416658G>C
NG_009809.2:g.416652G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.527-139G>C MANE Select	ENSP00000363680.4:n.527-139G>C
ENST00000374552.8:c.527-139G>C	ENSP00000363680.4:n.527-139G>C
ENST00000374553.6:c.527-139G>C	ENSP00000363681.2:n.527-139G>C
ENST00000503592.5:c.131-139G>C	ENSP00000423037.1:n.131-139G>C
ENST00000524573.5:c.527-139G>C	ENSP00000432585.1:n.527-139G>C
ENST00000616899.1:c.131-139G>C	ENSP00000481963.1:n.131-139G>C
NM_001005609.1:c.527-139G>C	NP_001005609.1:n.527-139G>C
NM_001005612.2:c.527-139G>C	NP_001005612.2:n.527-139G>C
NM_001399.4:c.527-139G>C	NP_001390.1:n.527-139G>C
XM_006724630.2:c.527-139G>C	XP_006724693.1:n.527-139G>C
XM_011530885.1:c.527-139G>C	XP_011529187.1:n.527-139G>C
XM_011530885.2:c.527-139G>C	XP_011529187.1:n.527-139G>C
XM_017029336.1:c.527-139G>C	XP_016884825.1:n.527-139G>C
NM_001399.5:c.527-139G>C MANE Select	NP_001390.1:n.527-139G>C
NM_001005609.2:c.527-139G>C	NP_001005609.1:n.527-139G>C
NM_001005612.3:c.527-139G>C	NP_001005612.2:n.527-139G>C