Canonical Allele Identifier: CA2669711023
Gene: MSANTD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256401_3256402del , CM000666.2:g.3256401_3256402del GRCh38
NC_000004.11:g.3258128_3258129del , CM000666.1:g.3258128_3258129del GRCh37
NC_000004.10:g.3227926_3227927del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000438480.7:c.*436_*437del MANE Select ENSP00000411584.2:n.*436_*437del
ENST00000505599.5:c.729+544_729+545del ENSP00000425405.1:n.729+544_729+545del
ENST00000507492.5:c.*436_*437del ENSP00000423547.1:n.*436_*437del
ENST00000510580.1:c.765+508_765+509del ENSP00000420966.1:n.765+508_765+509del
NM_001042690.1:c.*436_*437del NP_001036155.1:n.*436_*437del
XM_006713883.2:c.*436_*437del XP_006713946.1:n.*436_*437del
XM_011513464.1:c.729+544_729+545del XP_011511766.1:n.729+544_729+545del
XM_011513465.1:c.*436_*437del XP_011511767.1:n.*436_*437del
XM_011513466.1:c.*436_*437del XP_011511768.1:n.*436_*437del
XM_011513467.1:c.*436_*437del XP_011511769.1:n.*436_*437del
XR_924950.1:n.753+544_753+545del
NM_001330620.1:c.*436_*437del NP_001317549.1:n.*436_*437del
XM_011513466.3:c.*436_*437del XP_011511768.1:n.*436_*437del
XM_011513467.3:c.*436_*437del XP_011511769.1:n.*436_*437del
NM_001042690.2:c.*436_*437del MANE Select NP_001036155.1:n.*436_*437del
NM_001330620.2:c.*436_*437del NP_001317549.1:n.*436_*437del