Canonical Allele Identifier: CA1434131008
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1722403810

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256635del , CM000666.2:g.3256635del GRCh38
NC_000004.11:g.3258362del , CM000666.1:g.3258362del GRCh37
NC_000004.10:g.3228160del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+778del ENSP00000425405.1:n.729+778del
ENST00000510580.1:c.765+742del ENSP00000420966.1:n.765+742del
XM_011513464.1:c.729+778del XP_011511766.1:n.729+778del
XR_924950.1:n.753+778del