Canonical Allele Identifier: CA1034837344

Linked Data

dbSNP Id: rs1696599423

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108896676_108896677insAC , CM000664.2:g.108896676_108896677insAC GRCh38
NC_000002.11:g.109513132_109513133insAC , CM000664.1:g.109513132_109513133insAC GRCh37
NC_000002.10:g.108879564_108879565insAC NCBI36
NG_008257.1:g.97697_97698insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.*231_*232insTG (EDAR) MANE Select ENSP00000258443.2:n.*231_*232insTG
ENST00000258443.6:c.*231_*232insTG (EDAR) ENSP00000258443.2:n.*231_*232insTG
ENST00000376651.1:c.*231_*232insTG (EDAR) ENSP00000365839.1:n.*231_*232insTG
ENST00000409271.5:c.*231_*232insTG (EDAR) ENSP00000386371.1:n.*231_*232insTG
NM_022336.3:c.*231_*232insTG (EDAR) NP_071731.1:n.*231_*232insTG
XM_006712204.1:c.*231_*232insTG (EDAR) XP_006712267.1:n.*231_*232insTG
XM_011510502.1:c.*231_*232insTG (EDAR) XP_011508804.1:n.*231_*232insTG
XM_011510503.1:c.*231_*232insTG (EDAR) XP_011508805.1:n.*231_*232insTG
XM_011510504.1:c.*231_*232insTG (EDAR) XP_011508806.1:n.*231_*232insTG
XM_011510502.2:c.*231_*232insTG (EDAR) XP_011508804.2:n.*231_*232insTG
XM_011510503.2:c.*231_*232insTG (EDAR) XP_011508805.2:n.*231_*232insTG
XM_017004623.2:c.8370+123630_8370+123631insAC (RANBP2) XP_016860112.1:n.8370+123630_8370+123631insAC
NM_022336.4:c.*231_*232insTG (EDAR) MANE Select NP_071731.1:n.*231_*232insTG