Canonical Allele Identifier: CA212433169

Gene: SFR1

Linked Data

• dbSNP Id: rs773505118
• MyVariant Identifiers: chr10:g.105884103_105884104insA (hg19) ; chr10:g.104124345_104124346insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104124346dup , CM000672.2:g.104124346dup	GRCh38
NC_000010.10:g.105884104dup , CM000672.1:g.105884104dup	GRCh37
NC_000010.9:g.105874094dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369727.4:c.546+222dup MANE Select	ENSP00000358742.3:n.546+222dup
ENST00000369727.3:c.546+222dup	ENSP00000358742.3:n.546+222dup
ENST00000369729.7:c.507+222dup	ENSP00000358744.3:n.507+222dup
NM_001002759.1:c.546+222dup	NP_001002759.1:n.546+222dup
NM_145247.4:c.507+222dup	NP_660290.3:n.507+222dup
XM_005269521.2:c.732+222dup	XP_005269578.1:n.732+222dup
XM_005269521.3:c.732+222dup	XP_005269578.1:n.732+222dup
XM_017015672.1:c.507+222dup	XP_016871161.1:n.507+222dup
NM_001002759.2:c.546+222dup MANE Select	NP_001002759.1:n.546+222dup
NM_001384829.1:c.507+222dup	NP_001371758.1:n.507+222dup
NM_001384830.1:c.507+222dup	NP_001371759.1:n.507+222dup
NM_145247.5:c.507+222dup	NP_660290.3:n.507+222dup