Canonical Allele Identifier: CA2669711255
Gene: MSANTD1 HGNC NCBI

Linked Data

gnomAD v4: 4-3256614-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256614C>G , CM000666.2:g.3256614C>G GRCh38
NC_000004.11:g.3258341C>G , CM000666.1:g.3258341C>G GRCh37
NC_000004.10:g.3228139C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+757C>G ENSP00000425405.1:n.729+757C>G
ENST00000510580.1:c.765+721C>G ENSP00000420966.1:n.765+721C>G
NM_001042690.1:c.*649C>G NP_001036155.1:n.*649C>G
XM_011513464.1:c.729+757C>G XP_011511766.1:n.729+757C>G
XR_924950.1:n.753+757C>G