Canonical Allele Identifier: CA549307488
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1223015946
gnomAD v2: 4-3258516-T-TA
gnomAD v3: 4-3256789-T-TA
gnomAD v4: 4-3256789-T-TA

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256790dup , CM000666.2:g.3256790dup GRCh38
NC_000004.11:g.3258517dup , CM000666.1:g.3258517dup GRCh37
NC_000004.10:g.3228315dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+933dup ENSP00000425405.1:n.729+933dup
ENST00000510580.1:c.765+897dup ENSP00000420966.1:n.765+897dup
XM_011513464.1:c.729+933dup XP_011511766.1:n.729+933dup
XR_924950.1:n.753+933dup