Canonical Allele Identifier: CA1555785989

Gene: GFM2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74725543_74725548delinsCAAGAT , CM000667.2:g.74725543_74725548delinsCAAGAT	GRCh38
NC_000005.9:g.74021368_74021373delinsCAAGAT , CM000667.1:g.74021368_74021373delinsCAAGAT	GRCh37
NC_000005.8:g.74057124_74057129delinsCAAGAT	NCBI36
NG_011531.1:g.46670_46675delinsATCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2028+92_2028+97delinsATCTTG MANE Select	ENSP00000296805.3:n.2028+92_2028+97delinsATCTTG
ENST00000296805.7:c.2028+92_2028+97delinsATCTTG	ENSP00000296805.3:n.2028+92_2028+97delinsATCTTG
ENST00000345239.6:c.1887+92_1887+97delinsATCTTG	ENSP00000296804.3:n.1887+92_1887+97delinsATCTTG
ENST00000509430.5:c.2028+92_2028+97delinsATCTTG	ENSP00000427004.1:n.2028+92_2028+97delinsATCTTG
ENST00000515125.5:n.431+393_431+398delinsATCTTG
NM_001281302.1:c.2124+92_2124+97delinsATCTTG	NP_001268231.1:n.2124+92_2124+97delinsATCTTG
NM_032380.4:c.2028+92_2028+97delinsATCTTG	NP_115756.2:n.2028+92_2028+97delinsATCTTG
NM_170691.2:c.1887+92_1887+97delinsATCTTG	NP_733792.1:n.1887+92_1887+97delinsATCTTG
NR_104006.1:n.2347+92_2347+97delinsATCTTG
XM_006714721.2:c.1893+92_1893+97delinsATCTTG	XP_006714784.1:n.1893+92_1893+97delinsATCTTG
XM_011543690.1:c.2028+92_2028+97delinsATCTTG	XP_011541992.1:n.2028+92_2028+97delinsATCTTG
XM_017009986.1:c.2028+92_2028+97delinsATCTTG	XP_016865475.1:n.2028+92_2028+97delinsATCTTG
XR_002956185.1:n.3314+92_3314+97delinsATCTTG
NM_032380.5:c.2028+92_2028+97delinsATCTTG MANE Select	NP_115756.2:n.2028+92_2028+97delinsATCTTG
NM_001281302.2:c.2124+92_2124+97delinsATCTTG	NP_001268231.1:n.2124+92_2124+97delinsATCTTG
NM_170691.3:c.1887+92_1887+97delinsATCTTG	NP_733792.1:n.1887+92_1887+97delinsATCTTG
NR_104006.2:n.2093+92_2093+97delinsATCTTG