Canonical Allele Identifier: CA348047741

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513448A>G (hg19) ; chr2:g.108896992A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896992A>G , CM000664.2:g.108896992A>G	GRCh38
NC_000002.11:g.109513448A>G , CM000664.1:g.109513448A>G	GRCh37
NC_000002.10:g.108879880A>G	NCBI36
NG_008257.1:g.97381T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1262T>C (EDAR) MANE Select	ENSP00000258443.2:p.Leu421Pro
ENST00000258443.6:c.1262T>C (EDAR)	ENSP00000258443.2:p.Leu421Pro
ENST00000376651.1:c.1358T>C (EDAR)	ENSP00000365839.1:p.Leu453Pro
ENST00000409271.5:c.1358T>C (EDAR)	ENSP00000386371.1:p.Leu453Pro
NM_022336.3:c.1262T>C (EDAR)	NP_071731.1:p.Leu421Pro
XM_006712204.1:c.1358T>C (EDAR)	XP_006712267.1:p.Leu453Pro
XM_011510502.1:c.1409T>C (EDAR)	XP_011508804.1:p.Leu470Pro
XM_011510503.1:c.1313T>C (EDAR)	XP_011508805.1:p.Leu438Pro
XM_011510504.1:c.689T>C (EDAR)	XP_011508806.1:p.Leu230Pro
XM_011510502.2:c.1502T>C (EDAR)	XP_011508804.2:p.Leu501Pro
XM_011510503.2:c.1406T>C (EDAR)	XP_011508805.2:p.Leu469Pro
XM_017004623.2:c.8370+123946A>G (RANBP2)	XP_016860112.1:n.8370+123946A>G
NM_022336.4:c.1262T>C (EDAR) MANE Select	NP_071731.1:p.Leu421Pro