Canonical Allele Identifier: CA2778983781
Gene: MFHAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864770_8864771insTG , CM000670.2:g.8864770_8864771insTG GRCh38
NC_000008.10:g.8722280_8722281insTG , CM000670.1:g.8722280_8722281insTG GRCh37
NC_000008.9:g.8759690_8759691insTG NCBI36
NG_009444.1:g.33851_33852insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000276282.7:c.2998+25290_2998+25291insCA MANE Select ENSP00000276282.6:n.2998+25290_2998+25291insCA
ENST00000276282.6:c.2998+25290_2998+25291insCA ENSP00000276282.6:n.2998+25290_2998+25291insCA
NM_004225.2:c.2998+25290_2998+25291insCA NP_004216.2:n.2998+25290_2998+25291insCA
XR_246634.2:n.3534+25290_3534+25291insCA
XM_024447330.1:c.2998+25290_2998+25291insCA XP_024303098.1:n.2998+25290_2998+25291insCA
NM_004225.3:c.2998+25290_2998+25291insCA MANE Select NP_004216.2:n.2998+25290_2998+25291insCA