Canonical Allele Identifier: CA1434131019
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1722404347

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256653_3256655dup , CM000666.2:g.3256653_3256655dup GRCh38
NC_000004.11:g.3258380_3258382dup , CM000666.1:g.3258380_3258382dup GRCh37
NC_000004.10:g.3228178_3228180dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+796_729+798dup ENSP00000425405.1:n.729+796_729+798dup
ENST00000510580.1:c.765+760_765+762dup ENSP00000420966.1:n.765+760_765+762dup
XM_011513464.1:c.729+796_729+798dup XP_011511766.1:n.729+796_729+798dup
XR_924950.1:n.753+796_753+798dup