Canonical Allele Identifier: CA1933463681
Gene: SFR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104124305A= , CM000672.2:g.104124305A= GRCh38
NC_000010.10:g.105884063A= , CM000672.1:g.105884063A= GRCh37
NC_000010.9:g.105874053A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369727.4:c.546+181A= MANE Select ENSP00000358742.3:n.546+181A=
ENST00000369727.3:c.546+181A= ENSP00000358742.3:n.546+181A=
ENST00000369729.7:c.507+181A= ENSP00000358744.3:n.507+181A=
NM_001002759.1:c.546+181A= NP_001002759.1:n.546+181A=
NM_145247.4:c.507+181A= NP_660290.3:n.507+181A=
XM_005269521.2:c.732+181A= XP_005269578.1:n.732+181A=
XM_005269521.3:c.732+181A= XP_005269578.1:n.732+181A=
XM_017015672.1:c.507+181A= XP_016871161.1:n.507+181A=
NM_001002759.2:c.546+181A= MANE Select NP_001002759.1:n.546+181A=
NM_001384829.1:c.507+181A= NP_001371758.1:n.507+181A=
NM_001384830.1:c.507+181A= NP_001371759.1:n.507+181A=
NM_145247.5:c.507+181A= NP_660290.3:n.507+181A=