Canonical Allele Identifier: CA348050740

Gene: EDAR RANBP2

Linked Data

• dbSNP Id: rs1696841132
• gnomAD v4: 2-108907874-T-C
• MyVariant Identifiers: chr2:g.109524330T>C (hg19) ; chr2:g.108907874T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907874T>C , CM000664.2:g.108907874T>C	GRCh38
NC_000002.11:g.109524330T>C , CM000664.1:g.109524330T>C	GRCh37
NC_000002.10:g.108890762T>C	NCBI36
NG_008257.1:g.86499A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.949A>G (EDAR) MANE Select	ENSP00000258443.2:p.Asn317Asp
ENST00000258443.6:c.949A>G (EDAR)	ENSP00000258443.2:p.Asn317Asp
ENST00000376651.1:c.1045A>G (EDAR)	ENSP00000365839.1:p.Asn349Asp
ENST00000409271.5:c.1045A>G (EDAR)	ENSP00000386371.1:p.Asn349Asp
NM_022336.3:c.949A>G (EDAR)	NP_071731.1:p.Asn317Asp
XM_006712204.1:c.1045A>G (EDAR)	XP_006712267.1:p.Asn349Asp
XM_011510502.1:c.1096A>G (EDAR)	XP_011508804.1:p.Asn366Asp
XM_011510503.1:c.1000A>G (EDAR)	XP_011508805.1:p.Asn334Asp
XM_011510504.1:c.376A>G (EDAR)	XP_011508806.1:p.Asn126Asp
XM_011510502.2:c.1189A>G (EDAR)	XP_011508804.2:p.Asn397Asp
XM_011510503.2:c.1093A>G (EDAR)	XP_011508805.2:p.Asn365Asp
XM_017004623.2:c.8370+134828T>C (RANBP2)	XP_016860112.1:n.8370+134828T>C
NM_022336.4:c.949A>G (EDAR) MANE Select	NP_071731.1:p.Asn317Asp