Canonical Allele Identifier: CA1434131011
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256637G= , CM000666.2:g.3256637G= GRCh38
NC_000004.11:g.3258364G= , CM000666.1:g.3258364G= GRCh37
NC_000004.10:g.3228162G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+780G= ENSP00000425405.1:n.729+780G=
ENST00000510580.1:c.765+744G= ENSP00000420966.1:n.765+744G=
XM_011513464.1:c.729+780G= XP_011511766.1:n.729+780G=
XR_924950.1:n.753+780G=