Canonical Allele Identifier: CA1434130951
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256502A= , CM000666.2:g.3256502A= GRCh38
NC_000004.11:g.3258229A= , CM000666.1:g.3258229A= GRCh37
NC_000004.10:g.3228027A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438480.7:c.*537A= MANE Select ENSP00000411584.2:n.*537A=
ENST00000505599.5:c.729+645A= ENSP00000425405.1:n.729+645A=
ENST00000507492.5:c.*537A= ENSP00000423547.1:n.*537A=
ENST00000510580.1:c.765+609A= ENSP00000420966.1:n.765+609A=
NM_001042690.1:c.*537A= NP_001036155.1:n.*537A=
XM_006713883.2:c.*537A= XP_006713946.1:n.*537A=
XM_011513464.1:c.729+645A= XP_011511766.1:n.729+645A=
XM_011513465.1:c.*537A= XP_011511767.1:n.*537A=
XM_011513466.1:c.*537A= XP_011511768.1:n.*537A=
XM_011513467.1:c.*537A= XP_011511769.1:n.*537A=
XR_924950.1:n.753+645A=
NM_001330620.1:c.*537A= NP_001317549.1:n.*537A=
XM_011513466.3:c.*537A= XP_011511768.1:n.*537A=
XM_011513467.3:c.*537A= XP_011511769.1:n.*537A=
NM_001042690.2:c.*537A= MANE Select NP_001036155.1:n.*537A=
NM_001330620.2:c.*537A= NP_001317549.1:n.*537A=