Canonical Allele Identifier: CA1278354263

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897079G= , CM000664.2:g.108897079G=	GRCh38
NC_000002.11:g.109513535G= , CM000664.1:g.109513535G=	GRCh37
NC_000002.10:g.108879967G=	NCBI36
NG_008257.1:g.97294C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1175C= (EDAR) MANE Select	ENSP00000258443.2:p.Thr392=
ENST00000258443.6:c.1175C= (EDAR)	ENSP00000258443.2:p.Thr392=
ENST00000376651.1:c.1271C= (EDAR)	ENSP00000365839.1:p.Thr424=
ENST00000409271.5:c.1271C= (EDAR)	ENSP00000386371.1:p.Thr424=
NM_022336.3:c.1175C= (EDAR)	NP_071731.1:p.Thr392=
XM_006712204.1:c.1271C= (EDAR)	XP_006712267.1:p.Thr424=
XM_011510502.1:c.1322C= (EDAR)	XP_011508804.1:p.Thr441=
XM_011510503.1:c.1226C= (EDAR)	XP_011508805.1:p.Thr409=
XM_011510504.1:c.602C= (EDAR)	XP_011508806.1:p.Thr201=
XM_011510502.2:c.1415C= (EDAR)	XP_011508804.2:p.Thr472=
XM_011510503.2:c.1319C= (EDAR)	XP_011508805.2:p.Thr440=
XM_017004623.2:c.8370+124033G= (RANBP2)	XP_016860112.1:n.8370+124033G=
NM_022336.4:c.1175C= (EDAR) MANE Select	NP_071731.1:p.Thr392=