Canonical Allele Identifier: CA1434131083
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256791C= , CM000666.2:g.3256791C= GRCh38
NC_000004.11:g.3258518C= , CM000666.1:g.3258518C= GRCh37
NC_000004.10:g.3228316C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+934C= ENSP00000425405.1:n.729+934C=
ENST00000510580.1:c.765+898C= ENSP00000420966.1:n.765+898C=
XM_011513464.1:c.729+934C= XP_011511766.1:n.729+934C=
XR_924950.1:n.753+934C=