Canonical Allele Identifier: CA2682701

Gene: GFM1 LXN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.158666356C>T , CM000665.2:g.158666356C>T	GRCh38
NC_000003.11:g.158384145C>T , CM000665.1:g.158384145C>T	GRCh37
NC_000003.10:g.159866839C>T	NCBI36
NG_008441.1:g.26829C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024996.7:c.1571C>T (GFM1) MANE Select	NP_079272.4:p.Ala524Val
ENST00000486715.6:c.1571C>T (GFM1) MANE Select	ENSP00000419038.1:p.Ala524Val
NM_001308164.1:c.1628C>T (GFM1)	NP_001295093.1:p.Ala543Val
NM_001308164.2:c.1628C>T (GFM1)	NP_001295093.1:p.Ala543Val
NM_001308166.1:c.1571C>T (GFM1)	NP_001295095.1:p.Ala524Val
NM_001308166.2:c.1571C>T (GFM1)	NP_001295095.1:p.Ala524Val
NM_001374355.1:c.1490C>T (GFM1)	NP_001361284.1:p.Ala497Val
NM_001374356.1:c.1454C>T (GFM1)	NP_001361285.1:p.Ala485Val
NM_001374357.1:c.1346C>T (GFM1)	NP_001361286.1:p.Ala449Val
NM_001374358.1:c.1112C>T (GFM1)	NP_001361287.1:p.Ala371Val
NM_001374359.1:c.1004C>T (GFM1)	NP_001361288.1:p.Ala335Val
NM_001374360.1:c.1004C>T (GFM1)	NP_001361289.1:p.Ala335Val
NM_001374361.1:c.887C>T (GFM1)	NP_001361290.1:p.Ala296Val
NM_024996.5:c.1571C>T (GFM1)	NP_079272.4:p.Ala524Val
NR_164499.1:n.1594C>T (GFM1)
NR_164500.1:n.1679C>T (GFM1)
NR_164501.1:n.1224C>T (GFM1)
NR_164502.1:n.1558C>T (GFM1)
ENST00000264263.9:c.1628C>T (GFM1)	ENSP00000264263.5:p.Ala543Val
ENST00000478254.5:c.*211C>T (GFM1)	ENSP00000417225.1:n.*211C>T
ENST00000478576.5:c.1571C>T (GFM1)	ENSP00000418755.1:p.Ala524Val
ENST00000482640.5:c.361+656G>A (LXN)
ENST00000486715.5:c.1571C>T (GFM1)	ENSP00000419038.1:p.Ala524Val
XM_006713795.1:c.1454C>T (GFM1)	XP_006713858.1:p.Ala485Val
XM_006713795.2:c.1454C>T (GFM1)	XP_006713858.1:p.Ala485Val