Canonical Allele Identifier: CA2669711276
Gene: MSANTD1 HGNC NCBI

Linked Data

gnomAD v4: 4-3256639-TG-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256641del , CM000666.2:g.3256641del GRCh38
NC_000004.11:g.3258368del , CM000666.1:g.3258368del GRCh37
NC_000004.10:g.3228166del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+784del ENSP00000425405.1:n.729+784del
ENST00000510580.1:c.765+748del ENSP00000420966.1:n.765+748del
XM_011513464.1:c.729+784del XP_011511766.1:n.729+784del
XR_924950.1:n.753+784del