Canonical Allele Identifier: CA348048003

Linked Data

dbSNP Id: rs1696611032

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897053T>C , CM000664.2:g.108897053T>C GRCh38
NC_000002.11:g.109513509T>C , CM000664.1:g.109513509T>C GRCh37
NC_000002.10:g.108879941T>C NCBI36
NG_008257.1:g.97320A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.1201A>G (EDAR) MANE Select ENSP00000258443.2:p.Ile401Val
ENST00000258443.6:c.1201A>G (EDAR) ENSP00000258443.2:p.Ile401Val
ENST00000376651.1:c.1297A>G (EDAR) ENSP00000365839.1:p.Ile433Val
ENST00000409271.5:c.1297A>G (EDAR) ENSP00000386371.1:p.Ile433Val
NM_022336.3:c.1201A>G (EDAR) NP_071731.1:p.Ile401Val
XM_006712204.1:c.1297A>G (EDAR) XP_006712267.1:p.Ile433Val
XM_011510502.1:c.1348A>G (EDAR) XP_011508804.1:p.Ile450Val
XM_011510503.1:c.1252A>G (EDAR) XP_011508805.1:p.Ile418Val
XM_011510504.1:c.628A>G (EDAR) XP_011508806.1:p.Ile210Val
XM_011510502.2:c.1441A>G (EDAR) XP_011508804.2:p.Ile481Val
XM_011510503.2:c.1345A>G (EDAR) XP_011508805.2:p.Ile449Val
XM_017004623.2:c.8370+124007T>C (RANBP2) XP_016860112.1:n.8370+124007T>C
NM_022336.4:c.1201A>G (EDAR) MANE Select NP_071731.1:p.Ile401Val