Canonical Allele Identifier: CA1933463621

Gene: SFR1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104124211_104124212delinsAC , CM000672.2:g.104124211_104124212delinsAC	GRCh38
NC_000010.10:g.105883969_105883970delinsAC , CM000672.1:g.105883969_105883970delinsAC	GRCh37
NC_000010.9:g.105873959_105873960delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369727.4:c.546+87_546+88delinsAC MANE Select	ENSP00000358742.3:n.546+87_546+88delinsAC
ENST00000369727.3:c.546+87_546+88delinsAC	ENSP00000358742.3:n.546+87_546+88delinsAC
ENST00000369729.7:c.507+87_507+88delinsAC	ENSP00000358744.3:n.507+87_507+88delinsAC
NM_001002759.1:c.546+87_546+88delinsAC	NP_001002759.1:n.546+87_546+88delinsAC
NM_145247.4:c.507+87_507+88delinsAC	NP_660290.3:n.507+87_507+88delinsAC
XM_005269521.2:c.732+87_732+88delinsAC	XP_005269578.1:n.732+87_732+88delinsAC
XM_005269521.3:c.732+87_732+88delinsAC	XP_005269578.1:n.732+87_732+88delinsAC
XM_017015672.1:c.507+87_507+88delinsAC	XP_016871161.1:n.507+87_507+88delinsAC
NM_001002759.2:c.546+87_546+88delinsAC MANE Select	NP_001002759.1:n.546+87_546+88delinsAC
NM_001384829.1:c.507+87_507+88delinsAC	NP_001371758.1:n.507+87_507+88delinsAC
NM_001384830.1:c.507+87_507+88delinsAC	NP_001371759.1:n.507+87_507+88delinsAC
NM_145247.5:c.507+87_507+88delinsAC	NP_660290.3:n.507+87_507+88delinsAC