Canonical Allele Identifier: CA348048255

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513614A>T (hg19) ; chr2:g.108897158A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897158A>T , CM000664.2:g.108897158A>T	GRCh38
NC_000002.11:g.109513614A>T , CM000664.1:g.109513614A>T	GRCh37
NC_000002.10:g.108880046A>T	NCBI36
NG_008257.1:g.97215T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1096T>A (EDAR) MANE Select	ENSP00000258443.2:p.Ser366Thr
ENST00000258443.6:c.1096T>A (EDAR)	ENSP00000258443.2:p.Ser366Thr
ENST00000376651.1:c.1192T>A (EDAR)	ENSP00000365839.1:p.Ser398Thr
ENST00000409271.5:c.1192T>A (EDAR)	ENSP00000386371.1:p.Ser398Thr
NM_022336.3:c.1096T>A (EDAR)	NP_071731.1:p.Ser366Thr
XM_006712204.1:c.1192T>A (EDAR)	XP_006712267.1:p.Ser398Thr
XM_011510502.1:c.1243T>A (EDAR)	XP_011508804.1:p.Ser415Thr
XM_011510503.1:c.1147T>A (EDAR)	XP_011508805.1:p.Ser383Thr
XM_011510504.1:c.523T>A (EDAR)	XP_011508806.1:p.Ser175Thr
XM_011510502.2:c.1336T>A (EDAR)	XP_011508804.2:p.Ser446Thr
XM_011510503.2:c.1240T>A (EDAR)	XP_011508805.2:p.Ser414Thr
XM_017004623.2:c.8370+124112A>T (RANBP2)	XP_016860112.1:n.8370+124112A>T
NM_022336.4:c.1096T>A (EDAR) MANE Select	NP_071731.1:p.Ser366Thr