Canonical Allele Identifier: CA1434131121
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256861C= , CM000666.2:g.3256861C= GRCh38
NC_000004.11:g.3258588C= , CM000666.1:g.3258588C= GRCh37
NC_000004.10:g.3228386C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+1004C= ENSP00000425405.1:n.729+1004C=
ENST00000510580.1:c.765+968C= ENSP00000420966.1:n.765+968C=
XM_011513464.1:c.729+1004C= XP_011511766.1:n.729+1004C=
XR_924950.1:n.753+1004C=