Canonical Allele Identifier: CA348050948

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108907915A>T , CM000664.2:g.108907915A>T GRCh38
NC_000002.11:g.109524371A>T , CM000664.1:g.109524371A>T GRCh37
NC_000002.10:g.108890803A>T NCBI36
NG_008257.1:g.86458T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.908T>A (EDAR) MANE Select ENSP00000258443.2:p.Leu303Gln
ENST00000258443.6:c.908T>A (EDAR) ENSP00000258443.2:p.Leu303Gln
ENST00000376651.1:c.1004T>A (EDAR) ENSP00000365839.1:p.Leu335Gln
ENST00000409271.5:c.1004T>A (EDAR) ENSP00000386371.1:p.Leu335Gln
NM_022336.3:c.908T>A (EDAR) NP_071731.1:p.Leu303Gln
XM_006712204.1:c.1004T>A (EDAR) XP_006712267.1:p.Leu335Gln
XM_011510502.1:c.1055T>A (EDAR) XP_011508804.1:p.Leu352Gln
XM_011510503.1:c.959T>A (EDAR) XP_011508805.1:p.Leu320Gln
XM_011510504.1:c.335T>A (EDAR) XP_011508806.1:p.Leu112Gln
XM_011510502.2:c.1148T>A (EDAR) XP_011508804.2:p.Leu383Gln
XM_011510503.2:c.1052T>A (EDAR) XP_011508805.2:p.Leu351Gln
XM_017004623.2:c.8370+134869A>T (RANBP2) XP_016860112.1:n.8370+134869A>T
NM_022336.4:c.908T>A (EDAR) MANE Select NP_071731.1:p.Leu303Gln