Canonical Allele Identifier: CA348048044

Gene: EDAR RANBP2

Linked Data

• gnomAD v4: 2-108897070-A-G
• MyVariant Identifiers: chr2:g.109513526A>G (hg19) ; chr2:g.108897070A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897070A>G , CM000664.2:g.108897070A>G	GRCh38
NC_000002.11:g.109513526A>G , CM000664.1:g.109513526A>G	GRCh37
NC_000002.10:g.108879958A>G	NCBI36
NG_008257.1:g.97303T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1184T>C (EDAR) MANE Select	ENSP00000258443.2:p.Met395Thr
ENST00000258443.6:c.1184T>C (EDAR)	ENSP00000258443.2:p.Met395Thr
ENST00000376651.1:c.1280T>C (EDAR)	ENSP00000365839.1:p.Met427Thr
ENST00000409271.5:c.1280T>C (EDAR)	ENSP00000386371.1:p.Met427Thr
NM_022336.3:c.1184T>C (EDAR)	NP_071731.1:p.Met395Thr
XM_006712204.1:c.1280T>C (EDAR)	XP_006712267.1:p.Met427Thr
XM_011510502.1:c.1331T>C (EDAR)	XP_011508804.1:p.Met444Thr
XM_011510503.1:c.1235T>C (EDAR)	XP_011508805.1:p.Met412Thr
XM_011510504.1:c.611T>C (EDAR)	XP_011508806.1:p.Met204Thr
XM_011510502.2:c.1424T>C (EDAR)	XP_011508804.2:p.Met475Thr
XM_011510503.2:c.1328T>C (EDAR)	XP_011508805.2:p.Met443Thr
XM_017004623.2:c.8370+124024A>G (RANBP2)	XP_016860112.1:n.8370+124024A>G
NM_022336.4:c.1184T>C (EDAR) MANE Select	NP_071731.1:p.Met395Thr