Canonical Allele Identifier: CA424029805

Gene: EDARADD

Linked Data

• MyVariant Identifiers: chr1:g.236645604T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236482304T>A , CM000663.2:g.236482304T>A	GRCh38
NC_000001.10:g.236645604T>A , CM000663.1:g.236645604T>A	GRCh37
NC_000001.9:g.234712227T>A	NCBI36
NG_011566.1:g.92925T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334232.9:c.303T>A MANE Select	ENSP00000335076.4:p.Thr101=
ENST00000359362.6:c.273T>A	ENSP00000352320.4:p.Thr91=
ENST00000637660.1:c.237T>A	ENSP00000490347.1:p.Thr79=
ENST00000642595.1:c.236-9433T>A	ENSP00000494458.1:n.236-9433T>A
ENST00000334232.8:c.303T>A	ENSP00000335076.4:p.Thr101=
ENST00000359362.5:c.273T>A	ENSP00000352320.4:p.Thr91=
ENST00000439430.5:c.237T>A	ENSP00000405815.1:p.Thr79=
NM_080738.3:c.273T>A	NP_542776.1:p.Thr91=
NM_145861.2:c.303T>A	NP_665860.2:p.Thr101=
NM_080738.4:c.273T>A	NP_542776.1:p.Thr91=
NM_145861.4:c.303T>A MANE Select	NP_665860.2:p.Thr101=