Canonical Allele Identifier: CA1762279621
Gene: MFHAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864832_8864833delinsGA , CM000670.2:g.8864832_8864833delinsGA GRCh38
NC_000008.10:g.8722342_8722343delinsGA , CM000670.1:g.8722342_8722343delinsGA GRCh37
NC_000008.9:g.8759752_8759753delinsGA NCBI36
NG_009444.1:g.33789_33790delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000276282.7:c.2998+25228_2998+25229delinsTC MANE Select ENSP00000276282.6:n.2998+25228_2998+25229delinsTC
ENST00000276282.6:c.2998+25228_2998+25229delinsTC ENSP00000276282.6:n.2998+25228_2998+25229delinsTC
NM_004225.2:c.2998+25228_2998+25229delinsTC NP_004216.2:n.2998+25228_2998+25229delinsTC
XR_246634.2:n.3534+25228_3534+25229delinsTC
XM_024447330.1:c.2998+25228_2998+25229delinsTC XP_024303098.1:n.2998+25228_2998+25229delinsTC
NM_004225.3:c.2998+25228_2998+25229delinsTC MANE Select NP_004216.2:n.2998+25228_2998+25229delinsTC