Canonical Allele Identifier: CA1762279564
Gene: MFHAS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808793881

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864743dup , CM000670.2:g.8864743dup GRCh38
NC_000008.10:g.8722253dup , CM000670.1:g.8722253dup GRCh37
NC_000008.9:g.8759663dup NCBI36
NG_009444.1:g.33879dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000276282.7:c.2998+25318dup MANE Select ENSP00000276282.6:n.2998+25318dup
ENST00000276282.6:c.2998+25318dup ENSP00000276282.6:n.2998+25318dup
NM_004225.2:c.2998+25318dup NP_004216.2:n.2998+25318dup
XR_246634.2:n.3534+25318dup
XM_024447330.1:c.2998+25318dup XP_024303098.1:n.2998+25318dup
NM_004225.3:c.2998+25318dup MANE Select NP_004216.2:n.2998+25318dup