Canonical Allele Identifier: CA1278354300

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897150C= , CM000664.2:g.108897150C= GRCh38
NC_000002.11:g.109513606C= , CM000664.1:g.109513606C= GRCh37
NC_000002.10:g.108880038C= NCBI36
NG_008257.1:g.97223G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.1104G= (EDAR) MANE Select ENSP00000258443.2:p.Lys368=
ENST00000258443.6:c.1104G= (EDAR) ENSP00000258443.2:p.Lys368=
ENST00000376651.1:c.1200G= (EDAR) ENSP00000365839.1:p.Lys400=
ENST00000409271.5:c.1200G= (EDAR) ENSP00000386371.1:p.Lys400=
NM_022336.3:c.1104G= (EDAR) NP_071731.1:p.Lys368=
XM_006712204.1:c.1200G= (EDAR) XP_006712267.1:p.Lys400=
XM_011510502.1:c.1251G= (EDAR) XP_011508804.1:p.Lys417=
XM_011510503.1:c.1155G= (EDAR) XP_011508805.1:p.Lys385=
XM_011510504.1:c.531G= (EDAR) XP_011508806.1:p.Lys177=
XM_011510502.2:c.1344G= (EDAR) XP_011508804.2:p.Lys448=
XM_011510503.2:c.1248G= (EDAR) XP_011508805.2:p.Lys416=
XM_017004623.2:c.8370+124104C= (RANBP2) XP_016860112.1:n.8370+124104C=
NM_022336.4:c.1104G= (EDAR) MANE Select NP_071731.1:p.Lys368=