Canonical Allele Identifier: CA424029801

Gene: EDARADD

Linked Data

• MyVariant Identifiers: chr1:g.236645616C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236482316C>T , CM000663.2:g.236482316C>T	GRCh38
NC_000001.10:g.236645616C>T , CM000663.1:g.236645616C>T	GRCh37
NC_000001.9:g.234712239C>T	NCBI36
NG_011566.1:g.92937C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334232.9:c.315C>T MANE Select	ENSP00000335076.4:p.Cys105=
ENST00000359362.6:c.285C>T	ENSP00000352320.4:p.Cys95=
ENST00000637660.1:c.249C>T	ENSP00000490347.1:p.Cys83=
ENST00000642595.1:c.236-9421C>T	ENSP00000494458.1:n.236-9421C>T
ENST00000334232.8:c.315C>T	ENSP00000335076.4:p.Cys105=
ENST00000359362.5:c.285C>T	ENSP00000352320.4:p.Cys95=
ENST00000439430.5:c.249C>T	ENSP00000405815.1:p.Cys83=
NM_080738.3:c.285C>T	NP_542776.1:p.Cys95=
NM_145861.2:c.315C>T	NP_665860.2:p.Cys105=
NM_080738.4:c.285C>T	NP_542776.1:p.Cys95=
NM_145861.4:c.315C>T MANE Select	NP_665860.2:p.Cys105=