Canonical Allele Identifier: CA413449062

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69253373G>C (hg19) ; chrX:g.70033523G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033523G>C , CM000685.2:g.70033523G>C	GRCh38
NC_000023.10:g.69253373G>C , CM000685.1:g.69253373G>C	GRCh37
NC_000023.9:g.69170098G>C	NCBI36
NG_009809.1:g.422463G>C
NG_009809.2:g.422457G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.919G>C MANE Select	ENSP00000363680.4:p.Val307Leu
ENST00000374552.8:c.919G>C	ENSP00000363680.4:p.Val307Leu
ENST00000374553.6:c.918+1G>C	ENSP00000363681.2:n.918+1G>C
ENST00000524573.5:c.909+1G>C	ENSP00000432585.1:n.909+1G>C
ENST00000616899.1:c.523G>C	ENSP00000481963.1:p.Val175Leu
NM_001005609.1:c.918+1G>C	NP_001005609.1:n.918+1G>C
NM_001005612.2:c.909+1G>C	NP_001005612.2:n.909+1G>C
NM_001399.4:c.919G>C	NP_001390.1:p.Val307Leu
XM_006724630.2:c.910G>C	XP_006724693.1:p.Val304Leu
XM_011530885.1:c.918+1G>C	XP_011529187.1:n.918+1G>C
XM_011530885.2:c.918+1G>C	XP_011529187.1:n.918+1G>C
XM_017029336.1:c.882+37G>C	XP_016884825.1:n.882+37G>C
NM_001399.5:c.919G>C MANE Select	NP_001390.1:p.Val307Leu
NM_001005609.2:c.918+1G>C	NP_001005609.1:n.918+1G>C
NM_001005612.3:c.909+1G>C	NP_001005612.2:n.909+1G>C