Canonical Allele Identifier: CA2435957567

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.69957040_69957044delinsATTTC , CM000685.2:g.69957040_69957044delinsATTTC	GRCh38
NC_000023.10:g.69176890_69176894delinsATTTC , CM000685.1:g.69176890_69176894delinsATTTC	GRCh37
NC_000023.9:g.69093615_69093619delinsATTTC	NCBI36
NG_009809.1:g.345980_345984delinsATTTC
NG_009809.2:g.345974_345978delinsATTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.410_414delinsATTTC MANE Select	ENSP00000363680.4:p.Asn137=
ENST00000374548.5:n.652_656delinsATTTC
ENST00000374552.8:c.410_414delinsATTTC	ENSP00000363680.4:p.Asn137=
ENST00000374553.6:c.410_414delinsATTTC	ENSP00000363681.2:p.Asn137=
ENST00000502251.5:n.703_707delinsATTTC
ENST00000503592.5:c.14_18delinsATTTC	ENSP00000423037.1:p.Asn5=
ENST00000524573.5:c.410_414delinsATTTC	ENSP00000432585.1:p.Asn137=
ENST00000533317.5:n.1025_1029delinsATTTC
ENST00000616899.1:c.14_18delinsATTTC	ENSP00000481963.1:p.Asn5=
NM_001005609.1:c.410_414delinsATTTC	NP_001005609.1:p.Asn137=
NM_001005612.2:c.410_414delinsATTTC	NP_001005612.2:p.Asn137=
NM_001399.4:c.410_414delinsATTTC	NP_001390.1:p.Asn137=
XM_006724630.2:c.410_414delinsATTTC	XP_006724693.1:p.Asn137=
XM_011530885.1:c.410_414delinsATTTC	XP_011529187.1:p.Asn137=
XM_011530885.2:c.410_414delinsATTTC	XP_011529187.1:p.Asn137=
XM_017029336.1:c.410_414delinsATTTC	XP_016884825.1:p.Asn137=
NM_001399.5:c.410_414delinsATTTC MANE Select	NP_001390.1:p.Asn137=
NM_001005609.2:c.410_414delinsATTTC	NP_001005609.1:p.Asn137=
NM_001005612.3:c.410_414delinsATTTC	NP_001005612.2:p.Asn137=