Canonical Allele Identifier: CA1434131081
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256779G= , CM000666.2:g.3256779G= GRCh38
NC_000004.11:g.3258506G= , CM000666.1:g.3258506G= GRCh37
NC_000004.10:g.3228304G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+922G= ENSP00000425405.1:n.729+922G=
ENST00000510580.1:c.765+886G= ENSP00000420966.1:n.765+886G=
XM_011513464.1:c.729+922G= XP_011511766.1:n.729+922G=
XR_924950.1:n.753+922G=