Canonical Allele Identifier: CA1414368622

Gene: GFM1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.158645589A= , CM000665.2:g.158645589A=	GRCh38
NC_000003.11:g.158363378A= , CM000665.1:g.158363378A=	GRCh37
NC_000003.10:g.159846072A=	NCBI36
NG_008441.1:g.6062A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486715.6:c.82-40A= MANE Select	ENSP00000419038.1:n.82-40A=
ENST00000264263.9:c.82-40A=	ENSP00000264263.5:n.82-40A=
ENST00000464732.1:c.-144-40A=	ENSP00000417532.1:n.-144-40A=
ENST00000478254.5:c.82-40A=	ENSP00000417225.1:n.82-40A=
ENST00000478576.5:c.82-40A=	ENSP00000418755.1:n.82-40A=
ENST00000486715.5:c.82-40A=	ENSP00000419038.1:n.82-40A=
NM_001308164.1:c.82-40A=	NP_001295093.1:n.82-40A=
NM_001308166.1:c.82-40A=	NP_001295095.1:n.82-40A=
NM_024996.5:c.82-40A=	NP_079272.4:n.82-40A=
XM_006713795.1:c.82-40A=	XP_006713858.1:n.82-40A=
XM_006713795.2:c.82-40A=	XP_006713858.1:n.82-40A=
NM_001374355.1:c.82-40A=	NP_001361284.1:n.82-40A=
NM_001374356.1:c.82-40A=	NP_001361285.1:n.82-40A=
NM_001374357.1:c.-144-40A=	NP_001361286.1:n.-144-40A=
NM_001374358.1:c.82-40A=	NP_001361287.1:n.82-40A=
NM_001374359.1:c.-148-40A=	NP_001361288.1:n.-148-40A=
NM_001374360.1:c.-148-40A=	NP_001361289.1:n.-148-40A=
NM_001374361.1:c.-148-40A=	NP_001361290.1:n.-148-40A=
NM_024996.7:c.82-40A= MANE Select	NP_079272.4:n.82-40A=
NR_164499.1:n.190-40A=
NR_164500.1:n.190-40A=
NR_164501.1:n.190-40A=
NR_164502.1:n.190-40A=
NM_001308164.2:c.82-40A=	NP_001295093.1:n.82-40A=
NM_001308166.2:c.82-40A=	NP_001295095.1:n.82-40A=