Canonical Allele Identifier: CA1434130986
Gene: MSANTD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256585A= , CM000666.2:g.3256585A= GRCh38
NC_000004.11:g.3258312A= , CM000666.1:g.3258312A= GRCh37
NC_000004.10:g.3228110A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000438480.7:c.*620A= MANE Select ENSP00000411584.2:n.*620A=
ENST00000505599.5:c.729+728A= ENSP00000425405.1:n.729+728A=
ENST00000507492.5:c.*620A= ENSP00000423547.1:n.*620A=
ENST00000510580.1:c.765+692A= ENSP00000420966.1:n.765+692A=
NM_001042690.1:c.*620A= NP_001036155.1:n.*620A=
XM_006713883.2:c.*620A= XP_006713946.1:n.*620A=
XM_011513464.1:c.729+728A= XP_011511766.1:n.729+728A=
XM_011513465.1:c.*620A= XP_011511767.1:n.*620A=
XM_011513466.1:c.*620A= XP_011511768.1:n.*620A=
XM_011513467.1:c.*620A= XP_011511769.1:n.*620A=
XR_924950.1:n.753+728A=
NM_001330620.1:c.*620A= NP_001317549.1:n.*620A=
XM_011513466.3:c.*620A= XP_011511768.1:n.*620A=
XM_011513467.3:c.*620A= XP_011511769.1:n.*620A=
NM_001042690.2:c.*620A= MANE Select NP_001036155.1:n.*620A=
NM_001330620.2:c.*620A= NP_001317549.1:n.*620A=