Canonical Allele Identifier: CA2580101298

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.69957096_69957097delinsTC , CM000685.2:g.69957096_69957097delinsTC	GRCh38
NC_000023.10:g.69176946_69176947delinsTC , CM000685.1:g.69176946_69176947delinsTC	GRCh37
NC_000023.9:g.69093671_69093672delinsTC	NCBI36
NG_009809.1:g.346036_346037delinsTC
NG_009809.2:g.346030_346031delinsTC

Transcript Alleles

HGVS	Amino-acid Change
NM_001399.5:c.466_467delinsTC MANE Select	NP_001390.1:p.Arg156Ser
ENST00000374552.9:c.466_467delinsTC MANE Select	ENSP00000363680.4:p.Arg156Ser
NM_001005609.1:c.466_467delinsTC	NP_001005609.1:p.Arg156Ser
NM_001005609.2:c.466_467delinsTC	NP_001005609.1:p.Arg156Ser
NM_001005612.2:c.466_467delinsTC	NP_001005612.2:p.Arg156Ser
NM_001005612.3:c.466_467delinsTC	NP_001005612.2:p.Arg156Ser
NM_001399.4:c.466_467delinsTC	NP_001390.1:p.Arg156Ser
ENST00000374548.5:n.708_709delinsTC
ENST00000374552.8:c.466_467delinsTC	ENSP00000363680.4:p.Arg156Ser
ENST00000374553.6:c.466_467delinsTC	ENSP00000363681.2:p.Arg156Ser
ENST00000502251.5:n.759_760delinsTC
ENST00000503592.5:c.70_71delinsTC	ENSP00000423037.1:p.Arg24Ser
ENST00000524573.5:c.466_467delinsTC	ENSP00000432585.1:p.Arg156Ser
ENST00000533317.5:n.1081_1082delinsTC
ENST00000616899.1:c.70_71delinsTC	ENSP00000481963.1:p.Arg24Ser
XM_006724630.2:c.466_467delinsTC	XP_006724693.1:p.Arg156Ser
XM_011530885.1:c.466_467delinsTC	XP_011529187.1:p.Arg156Ser
XM_011530885.2:c.466_467delinsTC	XP_011529187.1:p.Arg156Ser
XM_017029336.1:c.466_467delinsTC	XP_016884825.1:p.Arg156Ser