Canonical Allele Identifier: CA348048532

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513665G>A (hg19) ; chr2:g.108897209G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897209G>A , CM000664.2:g.108897209G>A	GRCh38
NC_000002.11:g.109513665G>A , CM000664.1:g.109513665G>A	GRCh37
NC_000002.10:g.108880097G>A	NCBI36
NG_008257.1:g.97164C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1045C>T (EDAR) MANE Select	ENSP00000258443.2:p.Pro349Ser
ENST00000258443.6:c.1045C>T (EDAR)	ENSP00000258443.2:p.Pro349Ser
ENST00000376651.1:c.1141C>T (EDAR)	ENSP00000365839.1:p.Pro381Ser
ENST00000409271.5:c.1141C>T (EDAR)	ENSP00000386371.1:p.Pro381Ser
NM_022336.3:c.1045C>T (EDAR)	NP_071731.1:p.Pro349Ser
XM_006712204.1:c.1141C>T (EDAR)	XP_006712267.1:p.Pro381Ser
XM_011510502.1:c.1192C>T (EDAR)	XP_011508804.1:p.Pro398Ser
XM_011510503.1:c.1096C>T (EDAR)	XP_011508805.1:p.Pro366Ser
XM_011510504.1:c.472C>T (EDAR)	XP_011508806.1:p.Pro158Ser
XM_011510502.2:c.1285C>T (EDAR)	XP_011508804.2:p.Pro429Ser
XM_011510503.2:c.1189C>T (EDAR)	XP_011508805.2:p.Pro397Ser
XM_017004623.2:c.8370+124163G>A (RANBP2)	XP_016860112.1:n.8370+124163G>A
NM_022336.4:c.1045C>T (EDAR) MANE Select	NP_071731.1:p.Pro349Ser