Canonical Allele Identifier: CA1762279553

Gene: MFHAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.8864726_8864731delinsTCCTTG , CM000670.2:g.8864726_8864731delinsTCCTTG	GRCh38
NC_000008.10:g.8722236_8722241delinsTCCTTG , CM000670.1:g.8722236_8722241delinsTCCTTG	GRCh37
NC_000008.9:g.8759646_8759651delinsTCCTTG	NCBI36
NG_009444.1:g.33891_33896delinsCAAGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276282.7:c.2998+25330_2998+25335delinsCAAGGA MANE Select	ENSP00000276282.6:n.2998+25330_2998+25335delinsCAAGGA
ENST00000276282.6:c.2998+25330_2998+25335delinsCAAGGA	ENSP00000276282.6:n.2998+25330_2998+25335delinsCAAGGA
NM_004225.2:c.2998+25330_2998+25335delinsCAAGGA	NP_004216.2:n.2998+25330_2998+25335delinsCAAGGA
XR_246634.2:n.3534+25330_3534+25335delinsCAAGGA
XM_024447330.1:c.2998+25330_2998+25335delinsCAAGGA	XP_024303098.1:n.2998+25330_2998+25335delinsCAAGGA
NM_004225.3:c.2998+25330_2998+25335delinsCAAGGA MANE Select	NP_004216.2:n.2998+25330_2998+25335delinsCAAGGA