Canonical Allele Identifier: CA360072277

Gene: GFM2 HEXB

Linked Data

• MyVariant Identifiers: chr5:g.74017490C>A (hg19) ; chr5:g.74721665C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74721665C>A , CM000667.2:g.74721665C>A	GRCh38
NC_000005.9:g.74017490C>A , CM000667.1:g.74017490C>A	GRCh37
NC_000005.8:g.74053246C>A	NCBI36
NG_009770.1:g.41522C>A
NG_011531.1:g.50553G>T
NG_009770.2:g.86643C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2330G>T (GFM2) MANE Select	ENSP00000296805.3:p.Gly777Val
ENST00000296805.7:c.2330G>T (GFM2)	ENSP00000296805.3:p.Gly777Val
ENST00000345239.6:c.2189G>T (GFM2)	ENSP00000296804.3:p.Gly730Val
ENST00000503312.5:c.608+229C>A (HEXB)
ENST00000505859.1:c.255+229C>A (HEXB)
ENST00000509430.5:c.2330G>T (GFM2)	ENSP00000427004.1:p.Gly777Val
ENST00000513867.1:n.380+229C>A (HEXB)
ENST00000515125.5:n.733G>T (GFM2)
NM_001281302.1:c.2426G>T (GFM2)	NP_001268231.1:p.Gly809Val
NM_032380.4:c.2330G>T (GFM2)	NP_115756.2:p.Gly777Val
NM_170691.2:c.2189G>T (GFM2)	NP_733792.1:p.Gly730Val
NR_104006.1:n.2649G>T (GFM2)
XM_006714721.2:c.2195G>T (GFM2)	XP_006714784.1:p.Gly732Val
XM_011543690.1:c.2330G>T (GFM2)	XP_011541992.1:p.Gly777Val
XM_017009986.1:c.2330G>T (GFM2)	XP_016865475.1:p.Gly777Val
XR_002956185.1:n.3616G>T (GFM2)
NM_032380.5:c.2330G>T (GFM2) MANE Select	NP_115756.2:p.Gly777Val
NM_001281302.2:c.2426G>T (GFM2)	NP_001268231.1:p.Gly809Val
NM_170691.3:c.2189G>T (GFM2)	NP_733792.1:p.Gly730Val
NR_104006.2:n.2395G>T (GFM2)