Canonical Allele Identifier: CA1933463614

Gene: SFR1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104124199_104124200delinsAT , CM000672.2:g.104124199_104124200delinsAT	GRCh38
NC_000010.10:g.105883957_105883958delinsAT , CM000672.1:g.105883957_105883958delinsAT	GRCh37
NC_000010.9:g.105873947_105873948delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369727.4:c.546+75_546+76delinsAT MANE Select	ENSP00000358742.3:n.546+75_546+76delinsAT
ENST00000369727.3:c.546+75_546+76delinsAT	ENSP00000358742.3:n.546+75_546+76delinsAT
ENST00000369729.7:c.507+75_507+76delinsAT	ENSP00000358744.3:n.507+75_507+76delinsAT
NM_001002759.1:c.546+75_546+76delinsAT	NP_001002759.1:n.546+75_546+76delinsAT
NM_145247.4:c.507+75_507+76delinsAT	NP_660290.3:n.507+75_507+76delinsAT
XM_005269521.2:c.732+75_732+76delinsAT	XP_005269578.1:n.732+75_732+76delinsAT
XM_005269521.3:c.732+75_732+76delinsAT	XP_005269578.1:n.732+75_732+76delinsAT
XM_017015672.1:c.507+75_507+76delinsAT	XP_016871161.1:n.507+75_507+76delinsAT
NM_001002759.2:c.546+75_546+76delinsAT MANE Select	NP_001002759.1:n.546+75_546+76delinsAT
NM_001384829.1:c.507+75_507+76delinsAT	NP_001371758.1:n.507+75_507+76delinsAT
NM_001384830.1:c.507+75_507+76delinsAT	NP_001371759.1:n.507+75_507+76delinsAT
NM_145247.5:c.507+75_507+76delinsAT	NP_660290.3:n.507+75_507+76delinsAT