Canonical Allele Identifier: CA428203956

Linked Data

MyVariant Identifiers: chr2:g.109513467G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897011G>A , CM000664.2:g.108897011G>A GRCh38
NC_000002.11:g.109513467G>A , CM000664.1:g.109513467G>A GRCh37
NC_000002.10:g.108879899G>A NCBI36
NG_008257.1:g.97362C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.1243C>T (EDAR) MANE Select ENSP00000258443.2:p.Leu415=
ENST00000258443.6:c.1243C>T (EDAR) ENSP00000258443.2:p.Leu415=
ENST00000376651.1:c.1339C>T (EDAR) ENSP00000365839.1:p.Leu447=
ENST00000409271.5:c.1339C>T (EDAR) ENSP00000386371.1:p.Leu447=
NM_022336.3:c.1243C>T (EDAR) NP_071731.1:p.Leu415=
XM_006712204.1:c.1339C>T (EDAR) XP_006712267.1:p.Leu447=
XM_011510502.1:c.1390C>T (EDAR) XP_011508804.1:p.Leu464=
XM_011510503.1:c.1294C>T (EDAR) XP_011508805.1:p.Leu432=
XM_011510504.1:c.670C>T (EDAR) XP_011508806.1:p.Leu224=
XM_011510502.2:c.1483C>T (EDAR) XP_011508804.2:p.Leu495=
XM_011510503.2:c.1387C>T (EDAR) XP_011508805.2:p.Leu463=
XM_017004623.2:c.8370+123965G>A (RANBP2) XP_016860112.1:n.8370+123965G>A
NM_022336.4:c.1243C>T (EDAR) MANE Select NP_071731.1:p.Leu415=