Canonical Allele Identifier: CA345353863

Gene: EDARADD

Linked Data

• MyVariant Identifiers: chr1:g.236645708T>C (hg19) ; chr1:g.236482408T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236482408T>C , CM000663.2:g.236482408T>C	GRCh38
NC_000001.10:g.236645708T>C , CM000663.1:g.236645708T>C	GRCh37
NC_000001.9:g.234712331T>C	NCBI36
NG_011566.1:g.93029T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334232.9:c.407T>C MANE Select	ENSP00000335076.4:p.Val136Ala
ENST00000359362.6:c.377T>C	ENSP00000352320.4:p.Val126Ala
ENST00000637660.1:c.341T>C	ENSP00000490347.1:p.Val114Ala
ENST00000642595.1:c.236-9329T>C	ENSP00000494458.1:n.236-9329T>C
ENST00000334232.8:c.407T>C	ENSP00000335076.4:p.Val136Ala
ENST00000359362.5:c.377T>C	ENSP00000352320.4:p.Val126Ala
NM_080738.3:c.377T>C	NP_542776.1:p.Val126Ala
NM_145861.2:c.407T>C	NP_665860.2:p.Val136Ala
NM_080738.4:c.377T>C	NP_542776.1:p.Val126Ala
NM_145861.4:c.407T>C MANE Select	NP_665860.2:p.Val136Ala