Canonical Allele Identifier: CA2669711272
Gene: MSANTD1 HGNC NCBI

Linked Data

gnomAD v4: 4-3256636-T-TA

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256636_3256637insA , CM000666.2:g.3256636_3256637insA GRCh38
NC_000004.11:g.3258363_3258364insA , CM000666.1:g.3258363_3258364insA GRCh37
NC_000004.10:g.3228161_3228162insA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+779_729+780insA ENSP00000425405.1:n.729+779_729+780insA
ENST00000510580.1:c.765+743_765+744insA ENSP00000420966.1:n.765+743_765+744insA
XM_011513464.1:c.729+779_729+780insA XP_011511766.1:n.729+779_729+780insA
XR_924950.1:n.753+779_753+780insA