Canonical Allele Identifier: CA1077558994

Gene: GFM2 HEXB

Linked Data

• dbSNP Id: rs1749902724
• gnomAD v4: 5-74721845-C-CTGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74721847_74721850dup , CM000667.2:g.74721847_74721850dup	GRCh38
NC_000005.9:g.74017672_74017675dup , CM000667.1:g.74017672_74017675dup	GRCh37
NC_000005.8:g.74053428_74053431dup	NCBI36
NG_009770.1:g.41704_41707dup
NG_011531.1:g.50369_50372dup
NG_009770.2:g.86825_86828dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2212-66_2212-63dup (GFM2) MANE Select	ENSP00000296805.3:n.2212-66_2212-63dup
ENST00000296805.7:c.2212-66_2212-63dup (GFM2)	ENSP00000296805.3:n.2212-66_2212-63dup
ENST00000345239.6:c.2071-66_2071-63dup (GFM2)	ENSP00000296804.3:n.2071-66_2071-63dup
ENST00000503312.5:c.608+411_608+414dup (HEXB)
ENST00000505859.1:c.255+411_255+414dup (HEXB)
ENST00000509430.5:c.2212-66_2212-63dup (GFM2)	ENSP00000427004.1:n.2212-66_2212-63dup
ENST00000513867.1:n.380+411_380+414dup (HEXB)
ENST00000515125.5:n.615-66_615-63dup (GFM2)
NM_001281302.1:c.2308-66_2308-63dup (GFM2)	NP_001268231.1:n.2308-66_2308-63dup
NM_032380.4:c.2212-66_2212-63dup (GFM2)	NP_115756.2:n.2212-66_2212-63dup
NM_170691.2:c.2071-66_2071-63dup (GFM2)	NP_733792.1:n.2071-66_2071-63dup
NR_104006.1:n.2531-66_2531-63dup (GFM2)
XM_006714721.2:c.2077-66_2077-63dup (GFM2)	XP_006714784.1:n.2077-66_2077-63dup
XM_011543690.1:c.2212-66_2212-63dup (GFM2)	XP_011541992.1:n.2212-66_2212-63dup
XM_017009986.1:c.2212-66_2212-63dup (GFM2)	XP_016865475.1:n.2212-66_2212-63dup
XR_002956185.1:n.3498-66_3498-63dup (GFM2)
NM_032380.5:c.2212-66_2212-63dup (GFM2) MANE Select	NP_115756.2:n.2212-66_2212-63dup
NM_001281302.2:c.2308-66_2308-63dup (GFM2)	NP_001268231.1:n.2308-66_2308-63dup
NM_170691.3:c.2071-66_2071-63dup (GFM2)	NP_733792.1:n.2071-66_2071-63dup
NR_104006.2:n.2277-66_2277-63dup (GFM2)