Canonical Allele Identifier: CA549307500
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1340726990
gnomAD v2: 4-3258651-GT-G
gnomAD v3: 4-3256924-GT-G
gnomAD v4: 4-3256924-GT-G
MyVariant Identifiers: chr4:g.3258652del (hg19) chr4:g.3256925del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256925del , CM000666.2:g.3256925del GRCh38
NC_000004.11:g.3258652del , CM000666.1:g.3258652del GRCh37
NC_000004.10:g.3228450del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+1068del ENSP00000425405.1:n.729+1068del
ENST00000510580.1:c.765+1032del ENSP00000420966.1:n.765+1032del
XM_011513464.1:c.729+1068del XP_011511766.1:n.729+1068del
XR_924950.1:n.753+1068del
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