Canonical Allele Identifier: CA1933463605
Gene: SFR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104124181A= , CM000672.2:g.104124181A= GRCh38
NC_000010.10:g.105883939A= , CM000672.1:g.105883939A= GRCh37
NC_000010.9:g.105873929A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369727.4:c.546+57A= MANE Select ENSP00000358742.3:n.546+57A=
ENST00000369727.3:c.546+57A= ENSP00000358742.3:n.546+57A=
ENST00000369729.7:c.507+57A= ENSP00000358744.3:n.507+57A=
NM_001002759.1:c.546+57A= NP_001002759.1:n.546+57A=
NM_145247.4:c.507+57A= NP_660290.3:n.507+57A=
XM_005269521.2:c.732+57A= XP_005269578.1:n.732+57A=
XM_005269521.3:c.732+57A= XP_005269578.1:n.732+57A=
XM_017015672.1:c.507+57A= XP_016871161.1:n.507+57A=
NM_001002759.2:c.546+57A= MANE Select NP_001002759.1:n.546+57A=
NM_001384829.1:c.507+57A= NP_001371758.1:n.507+57A=
NM_001384830.1:c.507+57A= NP_001371759.1:n.507+57A=
NM_145247.5:c.507+57A= NP_660290.3:n.507+57A=