Canonical Allele Identifier: CA355175209

Gene: GFM1

Linked Data

• MyVariant Identifiers: chr3:g.158363478A>G (hg19) ; chr3:g.158645689A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.158645689A>G , CM000665.2:g.158645689A>G	GRCh38
NC_000003.11:g.158363478A>G , CM000665.1:g.158363478A>G	GRCh37
NC_000003.10:g.159846172A>G	NCBI36
NG_008441.1:g.6162A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000486715.6:c.142A>G MANE Select	ENSP00000419038.1:p.Asn48Asp
ENST00000264263.9:c.142A>G	ENSP00000264263.5:p.Asn48Asp
ENST00000464732.1:c.-84A>G	ENSP00000417532.1:n.-84A>G
ENST00000478254.5:c.142A>G	ENSP00000417225.1:p.Asn48Asp
ENST00000478576.5:c.142A>G	ENSP00000418755.1:p.Asn48Asp
ENST00000486715.5:c.142A>G	ENSP00000419038.1:p.Asn48Asp
NM_001308164.1:c.142A>G	NP_001295093.1:p.Asn48Asp
NM_001308166.1:c.142A>G	NP_001295095.1:p.Asn48Asp
NM_024996.5:c.142A>G	NP_079272.4:p.Asn48Asp
XM_006713795.1:c.142A>G	XP_006713858.1:p.Asn48Asp
XM_006713795.2:c.142A>G	XP_006713858.1:p.Asn48Asp
NM_001374355.1:c.142A>G	NP_001361284.1:p.Asn48Asp
NM_001374356.1:c.142A>G	NP_001361285.1:p.Asn48Asp
NM_001374357.1:c.-84A>G	NP_001361286.1:n.-84A>G
NM_001374358.1:c.142A>G	NP_001361287.1:p.Asn48Asp
NM_001374359.1:c.-88A>G	NP_001361288.1:n.-88A>G
NM_001374360.1:c.-88A>G	NP_001361289.1:n.-88A>G
NM_001374361.1:c.-88A>G	NP_001361290.1:n.-88A>G
NM_024996.7:c.142A>G MANE Select	NP_079272.4:p.Asn48Asp
NR_164499.1:n.250A>G
NR_164500.1:n.250A>G
NR_164501.1:n.250A>G
NR_164502.1:n.250A>G
NM_001308164.2:c.142A>G	NP_001295093.1:p.Asn48Asp
NM_001308166.2:c.142A>G	NP_001295095.1:p.Asn48Asp