Canonical Allele Identifier: CA2034421808
Gene: VDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47905029_47905030delinsCA , CM000674.2:g.47905029_47905030delinsCA GRCh38
NC_000012.11:g.48298812_48298813delinsCA , CM000674.1:g.48298812_48298813delinsCA GRCh37
NC_000012.10:g.46585079_46585080delinsCA NCBI36
NG_008731.1:g.5002_5003delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000229022.7:c.-281_-280delinsTG ENSP00000229022.3:n.-281_-280delinsTG
ENST00000395324.6:c.-83-22256_-83-22255delinsTG ENSP00000378734.2:n.-83-22256_-83-22255delinsTG
ENST00000548664.1:c.-281_-280delinsTG ENSP00000450105.1:n.-281_-280delinsTG
NM_000376.2:c.-159_-158delinsTG NP_000367.1:n.-159_-158delinsTG
NM_001017535.1:c.-281_-280delinsTG NP_001017535.1:n.-281_-280delinsTG
NM_001017536.1:c.-400_-399delinsTG NP_001017536.1:n.-400_-399delinsTG
NM_001364085.1:c.-159_-158delinsTG NP_001351014.1:n.-159_-158delinsTG