Canonical Allele Identifier: CA908138164

Gene: RFT1

Linked Data

• dbSNP Id: rs1437720273
• MyVariant Identifiers: chr3:g.53158077_53158078insA (hg19) ; chr3:g.53124061_53124062insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53124062dup , CM000665.2:g.53124062dup	GRCh38
NC_000003.11:g.53158078dup , CM000665.1:g.53158078dup	GRCh37
NC_000003.10:g.53133118dup	NCBI36
NG_009203.1:g.11393dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296292.8:c.150-222dup MANE Select	ENSP00000296292.3:n.150-222dup
ENST00000296292.7:c.150-222dup	ENSP00000296292.3:n.150-222dup
ENST00000394738.7:c.150-1499dup	ENSP00000378223.3:n.150-1499dup
ENST00000467048.1:c.150-222dup	ENSP00000420325.1:n.150-222dup
NM_052859.3:c.150-222dup	NP_443091.1:n.150-222dup
XM_005265537.3:c.150-222dup	XP_005265594.1:n.150-222dup
XM_006713384.2:c.150-222dup	XP_006713447.1:n.150-222dup
XM_011534214.1:c.150-222dup	XP_011532516.1:n.150-222dup
XM_011534215.1:c.150-222dup	XP_011532517.1:n.150-222dup
XR_940507.1:n.209-222dup
XM_005265537.4:c.150-222dup	XP_005265594.1:n.150-222dup
XM_006713384.3:c.150-222dup	XP_006713447.1:n.150-222dup
XM_011534214.2:c.150-222dup	XP_011532516.1:n.150-222dup
XM_011534215.3:c.150-222dup	XP_011532517.1:n.150-222dup
XM_011534216.3:c.-691-222dup	XP_011532518.1:n.-691-222dup
XM_017007460.1:c.150-222dup	XP_016862949.1:n.150-222dup
XM_017007461.2:c.-691-222dup	XP_016862950.1:n.-691-222dup
XR_001740360.2:n.216-222dup
NM_052859.4:c.150-222dup MANE Select	NP_443091.1:n.150-222dup