Canonical Allele Identifier: CA1824818

Linked Data

dbSNP Id: rs756272695

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897155C>T , CM000664.2:g.108897155C>T GRCh38
NC_000002.11:g.109513611C>T , CM000664.1:g.109513611C>T GRCh37
NC_000002.10:g.108880043C>T NCBI36
NG_008257.1:g.97218G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.1099G>A (EDAR) MANE Select ENSP00000258443.2:p.Glu367Lys
ENST00000258443.6:c.1099G>A (EDAR) ENSP00000258443.2:p.Glu367Lys
ENST00000376651.1:c.1195G>A (EDAR) ENSP00000365839.1:p.Glu399Lys
ENST00000409271.5:c.1195G>A (EDAR) ENSP00000386371.1:p.Glu399Lys
NM_022336.3:c.1099G>A (EDAR) NP_071731.1:p.Glu367Lys
XM_006712204.1:c.1195G>A (EDAR) XP_006712267.1:p.Glu399Lys
XM_011510502.1:c.1246G>A (EDAR) XP_011508804.1:p.Glu416Lys
XM_011510503.1:c.1150G>A (EDAR) XP_011508805.1:p.Glu384Lys
XM_011510504.1:c.526G>A (EDAR) XP_011508806.1:p.Glu176Lys
XM_011510502.2:c.1339G>A (EDAR) XP_011508804.2:p.Glu447Lys
XM_011510503.2:c.1243G>A (EDAR) XP_011508805.2:p.Glu415Lys
XM_017004623.2:c.8370+124109C>T (RANBP2) XP_016860112.1:n.8370+124109C>T
NM_022336.4:c.1099G>A (EDAR) MANE Select NP_071731.1:p.Glu367Lys