Canonical Allele Identifier: CA1367709328

Gene: FAM107A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58571114T= , CM000665.2:g.58571114T=	GRCh38
NC_000003.11:g.58556841T= , CM000665.1:g.58556841T=	GRCh37
NC_000003.10:g.58531881T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360997.7:c.-5-1249A= MANE Select	ENSP00000354270.2:n.-5-1249A=
ENST00000649301.1:c.-103-691A=	ENSP00000497152.1:n.-103-691A=
ENST00000360997.6:c.-5-1249A=	ENSP00000354270.2:n.-5-1249A=
ENST00000394481.5:c.-103-691A=	ENSP00000377991.1:n.-103-691A=
ENST00000447756.2:c.80-1249A=	ENSP00000400858.2:n.80-1249A=
ENST00000464064.5:c.-5-1249A=	ENSP00000419529.1:n.-5-1249A=
ENST00000465970.1:c.-5-1249A=	ENSP00000418038.1:n.-5-1249A=
ENST00000474531.5:c.89-1249A=	ENSP00000419124.1:n.89-1249A=
NM_001076778.2:c.-5-1249A=	NP_001070246.1:n.-5-1249A=
NM_001282713.1:c.80-1249A=	NP_001269642.1:n.80-1249A=
NM_001282714.1:c.89-1249A=	NP_001269643.1:n.89-1249A=
NM_007177.3:c.-103-691A=	NP_009108.1:n.-103-691A=
XM_005264835.2:c.-5-1249A=	XP_005264892.1:n.-5-1249A=
XR_001740721.1:n.278-1633T=
XR_001740722.2:n.685T=
XR_001740724.1:n.278-1633T=
NM_001076778.3:c.-5-1249A= MANE Select	NP_001070246.1:n.-5-1249A=
NM_001282713.2:c.80-1249A=	NP_001269642.1:n.80-1249A=
NM_001282714.2:c.89-1249A=	NP_001269643.1:n.89-1249A=
NM_007177.4:c.-103-691A=	NP_009108.1:n.-103-691A=