Canonical Allele Identifier: CA1434131013
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256639T= , CM000666.2:g.3256639T= GRCh38
NC_000004.11:g.3258366T= , CM000666.1:g.3258366T= GRCh37
NC_000004.10:g.3228164T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+782T= ENSP00000425405.1:n.729+782T=
ENST00000510580.1:c.765+746T= ENSP00000420966.1:n.765+746T=
XM_011513464.1:c.729+782T= XP_011511766.1:n.729+782T=
XR_924950.1:n.753+782T=