Canonical Allele Identifier: CA1434131085
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256796A= , CM000666.2:g.3256796A= GRCh38
NC_000004.11:g.3258523A= , CM000666.1:g.3258523A= GRCh37
NC_000004.10:g.3228321A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+939A= ENSP00000425405.1:n.729+939A=
ENST00000510580.1:c.765+903A= ENSP00000420966.1:n.765+903A=
XM_011513464.1:c.729+939A= XP_011511766.1:n.729+939A=
XR_924950.1:n.753+939A=