Canonical Allele Identifier: CA1434131045
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256699G= , CM000666.2:g.3256699G= GRCh38
NC_000004.11:g.3258426G= , CM000666.1:g.3258426G= GRCh37
NC_000004.10:g.3228224G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+842G= ENSP00000425405.1:n.729+842G=
ENST00000510580.1:c.765+806G= ENSP00000420966.1:n.765+806G=
XM_011513464.1:c.729+842G= XP_011511766.1:n.729+842G=
XR_924950.1:n.753+842G=