Canonical Allele Identifier: CA1434131104
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256828A= , CM000666.2:g.3256828A= GRCh38
NC_000004.11:g.3258555A= , CM000666.1:g.3258555A= GRCh37
NC_000004.10:g.3228353A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+971A= ENSP00000425405.1:n.729+971A=
ENST00000510580.1:c.765+935A= ENSP00000420966.1:n.765+935A=
XM_011513464.1:c.729+971A= XP_011511766.1:n.729+971A=
XR_924950.1:n.753+971A=