Canonical Allele Identifier: CA1278369381

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108930982G= , CM000664.2:g.108930982G=	GRCh38
NC_000002.11:g.109547438G= , CM000664.1:g.109547438G=	GRCh37
NC_000002.10:g.108913870G=	NCBI36
NG_008257.1:g.63391C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.33C= (EDAR) MANE Select	ENSP00000258443.2:p.Pro11=
ENST00000258443.6:c.33C= (EDAR)	ENSP00000258443.2:p.Pro11=
ENST00000376651.1:c.33C= (EDAR)	ENSP00000365839.1:p.Pro11=
ENST00000409271.5:c.33C= (EDAR)	ENSP00000386371.1:p.Pro11=
NM_022336.3:c.33C= (EDAR)	NP_071731.1:p.Pro11=
XM_006712204.1:c.33C= (EDAR)	XP_006712267.1:p.Pro11=
XM_011510502.1:c.84C= (EDAR)	XP_011508804.1:p.Pro28=
XM_011510503.1:c.84C= (EDAR)	XP_011508805.1:p.Pro28=
XM_011510502.2:c.177C= (EDAR)	XP_011508804.2:p.Pro59=
XM_011510503.2:c.177C= (EDAR)	XP_011508805.2:p.Pro59=
XM_017004623.2:c.8370+157936G= (RANBP2)	XP_016860112.1:n.8370+157936G=
NM_022336.4:c.33C= (EDAR) MANE Select	NP_071731.1:p.Pro11=