Canonical Allele Identifier: CA424029867

Gene: EDARADD

Linked Data

• gnomAD v4: 1-236482415-C-T
• MyVariant Identifiers: chr1:g.236645715C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236482415C>T , CM000663.2:g.236482415C>T	GRCh38
NC_000001.10:g.236645715C>T , CM000663.1:g.236645715C>T	GRCh37
NC_000001.9:g.234712338C>T	NCBI36
NG_011566.1:g.93036C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334232.9:c.414C>T MANE Select	ENSP00000335076.4:p.Asn138=
ENST00000359362.6:c.384C>T	ENSP00000352320.4:p.Asn128=
ENST00000637660.1:c.348C>T	ENSP00000490347.1:p.Asn116=
ENST00000642595.1:c.236-9322C>T	ENSP00000494458.1:n.236-9322C>T
ENST00000334232.8:c.414C>T	ENSP00000335076.4:p.Asn138=
ENST00000359362.5:c.384C>T	ENSP00000352320.4:p.Asn128=
NM_080738.3:c.384C>T	NP_542776.1:p.Asn128=
NM_145861.2:c.414C>T	NP_665860.2:p.Asn138=
NM_080738.4:c.384C>T	NP_542776.1:p.Asn128=
NM_145861.4:c.414C>T MANE Select	NP_665860.2:p.Asn138=