Canonical Allele Identifier: CA1434131122
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256864G= , CM000666.2:g.3256864G= GRCh38
NC_000004.11:g.3258591G= , CM000666.1:g.3258591G= GRCh37
NC_000004.10:g.3228389G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+1007G= ENSP00000425405.1:n.729+1007G=
ENST00000510580.1:c.765+971G= ENSP00000420966.1:n.765+971G=
XM_011513464.1:c.729+1007G= XP_011511766.1:n.729+1007G=
XR_924950.1:n.753+1007G=