Canonical Allele Identifier: CA1762279495

Gene: MFHAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.8864622T= , CM000670.2:g.8864622T=	GRCh38
NC_000008.10:g.8722132T= , CM000670.1:g.8722132T=	GRCh37
NC_000008.9:g.8759542T=	NCBI36
NG_009444.1:g.34000A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276282.7:c.2998+25439A= MANE Select	ENSP00000276282.6:n.2998+25439A=
ENST00000276282.6:c.2998+25439A=	ENSP00000276282.6:n.2998+25439A=
NM_004225.2:c.2998+25439A=	NP_004216.2:n.2998+25439A=
XR_246634.2:n.3534+25439A=
XM_024447330.1:c.2998+25439A=	XP_024303098.1:n.2998+25439A=
NM_004225.3:c.2998+25439A= MANE Select	NP_004216.2:n.2998+25439A=