Canonical Allele Identifier: CA1434131096
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256810G= , CM000666.2:g.3256810G= GRCh38
NC_000004.11:g.3258537G= , CM000666.1:g.3258537G= GRCh37
NC_000004.10:g.3228335G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+953G= ENSP00000425405.1:n.729+953G=
ENST00000510580.1:c.765+917G= ENSP00000420966.1:n.765+917G=
XM_011513464.1:c.729+953G= XP_011511766.1:n.729+953G=
XR_924950.1:n.753+953G=