Canonical Allele Identifier: CA2660593126

Gene: EDAR RANBP2

Linked Data

• gnomAD v4: 2-108896799-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896799A>G , CM000664.2:g.108896799A>G	GRCh38
NC_000002.11:g.109513255A>G , CM000664.1:g.109513255A>G	GRCh37
NC_000002.10:g.108879687A>G	NCBI36
NG_008257.1:g.97574T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.*108T>C (EDAR) MANE Select	ENSP00000258443.2:n.*108T>C
ENST00000258443.6:c.*108T>C (EDAR)	ENSP00000258443.2:n.*108T>C
ENST00000376651.1:c.*108T>C (EDAR)	ENSP00000365839.1:n.*108T>C
ENST00000409271.5:c.*108T>C (EDAR)	ENSP00000386371.1:n.*108T>C
NM_022336.3:c.*108T>C (EDAR)	NP_071731.1:n.*108T>C
XM_006712204.1:c.*108T>C (EDAR)	XP_006712267.1:n.*108T>C
XM_011510502.1:c.*108T>C (EDAR)	XP_011508804.1:n.*108T>C
XM_011510503.1:c.*108T>C (EDAR)	XP_011508805.1:n.*108T>C
XM_011510504.1:c.*108T>C (EDAR)	XP_011508806.1:n.*108T>C
XM_011510502.2:c.*108T>C (EDAR)	XP_011508804.2:n.*108T>C
XM_011510503.2:c.*108T>C (EDAR)	XP_011508805.2:n.*108T>C
XM_017004623.2:c.8370+123753A>G (RANBP2)	XP_016860112.1:n.8370+123753A>G
NM_022336.4:c.*108T>C (EDAR) MANE Select	NP_071731.1:n.*108T>C