Canonical Allele Identifier: CA1434130998
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256615A= , CM000666.2:g.3256615A= GRCh38
NC_000004.11:g.3258342A= , CM000666.1:g.3258342A= GRCh37
NC_000004.10:g.3228140A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+758A= ENSP00000425405.1:n.729+758A=
ENST00000510580.1:c.765+722A= ENSP00000420966.1:n.765+722A=
NM_001042690.1:c.*650A= NP_001036155.1:n.*650A=
XM_011513464.1:c.729+758A= XP_011511766.1:n.729+758A=
XR_924950.1:n.753+758A=