Canonical Allele Identifier: CA1278354219

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108896964G= , CM000664.2:g.108896964G= GRCh38
NC_000002.11:g.109513420G= , CM000664.1:g.109513420G= GRCh37
NC_000002.10:g.108879852G= NCBI36
NG_008257.1:g.97409C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.1290C= (EDAR) MANE Select ENSP00000258443.2:p.Asp430=
ENST00000258443.6:c.1290C= (EDAR) ENSP00000258443.2:p.Asp430=
ENST00000376651.1:c.1386C= (EDAR) ENSP00000365839.1:p.Asp462=
ENST00000409271.5:c.1386C= (EDAR) ENSP00000386371.1:p.Asp462=
NM_022336.3:c.1290C= (EDAR) NP_071731.1:p.Asp430=
XM_006712204.1:c.1386C= (EDAR) XP_006712267.1:p.Asp462=
XM_011510502.1:c.1437C= (EDAR) XP_011508804.1:p.Asp479=
XM_011510503.1:c.1341C= (EDAR) XP_011508805.1:p.Asp447=
XM_011510504.1:c.717C= (EDAR) XP_011508806.1:p.Asp239=
XM_011510502.2:c.1530C= (EDAR) XP_011508804.2:p.Asp510=
XM_011510503.2:c.1434C= (EDAR) XP_011508805.2:p.Asp478=
XM_017004623.2:c.8370+123918G= (RANBP2) XP_016860112.1:n.8370+123918G=
NM_022336.4:c.1290C= (EDAR) MANE Select NP_071731.1:p.Asp430=