Canonical Allele Identifier: CA794017915
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1481967800

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256648_3256650del , CM000666.2:g.3256648_3256650del GRCh38
NC_000004.11:g.3258375_3258377del , CM000666.1:g.3258375_3258377del GRCh37
NC_000004.10:g.3228173_3228175del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+791_729+793del ENSP00000425405.1:n.729+791_729+793del
ENST00000510580.1:c.765+755_765+757del ENSP00000420966.1:n.765+755_765+757del
XM_011513464.1:c.729+791_729+793del XP_011511766.1:n.729+791_729+793del
XR_924950.1:n.753+791_753+793del