Canonical Allele Identifier: CA2674243562

Gene: GFM2

Linked Data

• gnomAD v4: 5-74725533-GGCAAAGACACAAGATAAGGCTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74725535_74725557del , CM000667.2:g.74725535_74725557del	GRCh38
NC_000005.9:g.74021360_74021382del , CM000667.1:g.74021360_74021382del	GRCh37
NC_000005.8:g.74057116_74057138del	NCBI36
NG_011531.1:g.46662_46684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2028+84_2028+106del MANE Select	ENSP00000296805.3:n.2028+84_2028+106del
ENST00000296805.7:c.2028+84_2028+106del	ENSP00000296805.3:n.2028+84_2028+106del
ENST00000345239.6:c.1887+84_1887+106del	ENSP00000296804.3:n.1887+84_1887+106del
ENST00000509430.5:c.2028+84_2028+106del	ENSP00000427004.1:n.2028+84_2028+106del
ENST00000515125.5:n.431+385_431+407del
NM_001281302.1:c.2124+84_2124+106del	NP_001268231.1:n.2124+84_2124+106del
NM_032380.4:c.2028+84_2028+106del	NP_115756.2:n.2028+84_2028+106del
NM_170691.2:c.1887+84_1887+106del	NP_733792.1:n.1887+84_1887+106del
NR_104006.1:n.2347+84_2347+106del
XM_006714721.2:c.1893+84_1893+106del	XP_006714784.1:n.1893+84_1893+106del
XM_011543690.1:c.2028+84_2028+106del	XP_011541992.1:n.2028+84_2028+106del
XM_017009986.1:c.2028+84_2028+106del	XP_016865475.1:n.2028+84_2028+106del
XR_002956185.1:n.3314+84_3314+106del
NM_032380.5:c.2028+84_2028+106del MANE Select	NP_115756.2:n.2028+84_2028+106del
NM_001281302.2:c.2124+84_2124+106del	NP_001268231.1:n.2124+84_2124+106del
NM_170691.3:c.1887+84_1887+106del	NP_733792.1:n.1887+84_1887+106del
NR_104006.2:n.2093+84_2093+106del