Canonical Allele Identifier: CA1434131006
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256631C= , CM000666.2:g.3256631C= GRCh38
NC_000004.11:g.3258358C= , CM000666.1:g.3258358C= GRCh37
NC_000004.10:g.3228156C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+774C= ENSP00000425405.1:n.729+774C=
ENST00000510580.1:c.765+738C= ENSP00000420966.1:n.765+738C=
XM_011513464.1:c.729+774C= XP_011511766.1:n.729+774C=
XR_924950.1:n.753+774C=