Canonical Allele Identifier: CA444849819

Gene: GFM2 HEXB

Linked Data

• MyVariant Identifiers: chr5:g.74017489A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74721664A>C , CM000667.2:g.74721664A>C	GRCh38
NC_000005.9:g.74017489A>C , CM000667.1:g.74017489A>C	GRCh37
NC_000005.8:g.74053245A>C	NCBI36
NG_009770.1:g.41521A>C
NG_011531.1:g.50554T>G
NG_009770.2:g.86642A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2331T>G (GFM2) MANE Select	ENSP00000296805.3:p.Gly777=
ENST00000296805.7:c.2331T>G (GFM2)	ENSP00000296805.3:p.Gly777=
ENST00000345239.6:c.2190T>G (GFM2)	ENSP00000296804.3:p.Gly730=
ENST00000503312.5:c.608+228A>C (HEXB)
ENST00000505859.1:c.255+228A>C (HEXB)
ENST00000509430.5:c.2331T>G (GFM2)	ENSP00000427004.1:p.Gly777=
ENST00000513867.1:n.380+228A>C (HEXB)
ENST00000515125.5:n.734T>G (GFM2)
NM_001281302.1:c.2427T>G (GFM2)	NP_001268231.1:p.Gly809=
NM_032380.4:c.2331T>G (GFM2)	NP_115756.2:p.Gly777=
NM_170691.2:c.2190T>G (GFM2)	NP_733792.1:p.Gly730=
NR_104006.1:n.2650T>G (GFM2)
XM_006714721.2:c.2196T>G (GFM2)	XP_006714784.1:p.Gly732=
XM_011543690.1:c.2331T>G (GFM2)	XP_011541992.1:p.Gly777=
XM_017009986.1:c.2331T>G (GFM2)	XP_016865475.1:p.Gly777=
XR_002956185.1:n.3617T>G (GFM2)
NM_032380.5:c.2331T>G (GFM2) MANE Select	NP_115756.2:p.Gly777=
NM_001281302.2:c.2427T>G (GFM2)	NP_001268231.1:p.Gly809=
NM_170691.3:c.2190T>G (GFM2)	NP_733792.1:p.Gly730=
NR_104006.2:n.2396T>G (GFM2)