Canonical Allele Identifier: CA120915394

Gene: GFM2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74732972_74732979del , CM000667.2:g.74732972_74732979del	GRCh38
NC_000005.9:g.74028797_74028804del , CM000667.1:g.74028797_74028804del	GRCh37
NC_000005.8:g.74064553_74064560del	NCBI36
NG_011531.1:g.39283_39290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.1587+87_1587+94del MANE Select	ENSP00000296805.3:n.1587+87_1587+94del
ENST00000296805.7:c.1587+87_1587+94del	ENSP00000296805.3:n.1587+87_1587+94del
ENST00000345239.6:c.1446+87_1446+94del	ENSP00000296804.3:n.1446+87_1446+94del
ENST00000506263.1:n.367+87_367+94del
ENST00000509430.5:c.1587+87_1587+94del	ENSP00000427004.1:n.1587+87_1587+94del
ENST00000514734.5:n.324+87_324+94del
ENST00000515125.5:n.245+87_245+94del
NM_001281302.1:c.1683+87_1683+94del	NP_001268231.1:n.1683+87_1683+94del
NM_032380.4:c.1587+87_1587+94del	NP_115756.2:n.1587+87_1587+94del
NM_170691.2:c.1446+87_1446+94del	NP_733792.1:n.1446+87_1446+94del
NR_104006.1:n.2045+87_2045+94del
XM_006714721.2:c.1591+83_1591+90del	XP_006714784.1:n.1591+83_1591+90del
XM_011543690.1:c.1587+87_1587+94del	XP_011541992.1:n.1587+87_1587+94del
XM_011543691.1:c.1587+87_1587+94del	XP_011541993.1:n.1587+87_1587+94del
XM_011543691.3:c.1587+87_1587+94del	XP_011541993.1:n.1587+87_1587+94del
XM_017009986.1:c.1587+87_1587+94del	XP_016865475.1:n.1587+87_1587+94del
XR_002956185.1:n.3012+87_3012+94del
NM_032380.5:c.1587+87_1587+94del MANE Select	NP_115756.2:n.1587+87_1587+94del
NM_001281302.2:c.1683+87_1683+94del	NP_001268231.1:n.1683+87_1683+94del
NM_170691.3:c.1446+87_1446+94del	NP_733792.1:n.1446+87_1446+94del
NR_104006.2:n.1791+87_1791+94del