Canonical Allele Identifier: CA2674243610

Gene: GFM2

Linked Data

• gnomAD v4: 5-74725591-TACTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74725593_74725596del , CM000667.2:g.74725593_74725596del	GRCh38
NC_000005.9:g.74021418_74021421del , CM000667.1:g.74021418_74021421del	GRCh37
NC_000005.8:g.74057174_74057177del	NCBI36
NG_011531.1:g.46623_46626del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2028+45_2028+48del MANE Select	ENSP00000296805.3:n.2028+45_2028+48del
ENST00000296805.7:c.2028+45_2028+48del	ENSP00000296805.3:n.2028+45_2028+48del
ENST00000345239.6:c.1887+45_1887+48del	ENSP00000296804.3:n.1887+45_1887+48del
ENST00000509430.5:c.2028+45_2028+48del	ENSP00000427004.1:n.2028+45_2028+48del
ENST00000515125.5:n.431+346_431+349del
NM_001281302.1:c.2124+45_2124+48del	NP_001268231.1:n.2124+45_2124+48del
NM_032380.4:c.2028+45_2028+48del	NP_115756.2:n.2028+45_2028+48del
NM_170691.2:c.1887+45_1887+48del	NP_733792.1:n.1887+45_1887+48del
NR_104006.1:n.2347+45_2347+48del
XM_006714721.2:c.1893+45_1893+48del	XP_006714784.1:n.1893+45_1893+48del
XM_011543690.1:c.2028+45_2028+48del	XP_011541992.1:n.2028+45_2028+48del
XM_017009986.1:c.2028+45_2028+48del	XP_016865475.1:n.2028+45_2028+48del
XR_002956185.1:n.3314+45_3314+48del
NM_032380.5:c.2028+45_2028+48del MANE Select	NP_115756.2:n.2028+45_2028+48del
NM_001281302.2:c.2124+45_2124+48del	NP_001268231.1:n.2124+45_2124+48del
NM_170691.3:c.1887+45_1887+48del	NP_733792.1:n.1887+45_1887+48del
NR_104006.2:n.2093+45_2093+48del