Canonical Allele Identifier: CA360076274

Gene: GFM2

Linked Data

• MyVariant Identifiers: chr5:g.74021541G>T (hg19) ; chr5:g.74725716G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74725716G>T , CM000667.2:g.74725716G>T	GRCh38
NC_000005.9:g.74021541G>T , CM000667.1:g.74021541G>T	GRCh37
NC_000005.8:g.74057297G>T	NCBI36
NG_011531.1:g.46502C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.1952C>A MANE Select	ENSP00000296805.3:p.Thr651Asn
ENST00000296805.7:c.1952C>A	ENSP00000296805.3:p.Thr651Asn
ENST00000345239.6:c.1811C>A	ENSP00000296804.3:p.Thr604Asn
ENST00000509430.5:c.1952C>A	ENSP00000427004.1:p.Thr651Asn
ENST00000514734.5:n.863C>A
ENST00000515125.5:n.431+225C>A
NM_001281302.1:c.2048C>A	NP_001268231.1:p.Thr683Asn
NM_032380.4:c.1952C>A	NP_115756.2:p.Thr651Asn
NM_170691.2:c.1811C>A	NP_733792.1:p.Thr604Asn
NR_104006.1:n.2271C>A
XM_006714721.2:c.1817C>A	XP_006714784.1:p.Thr606Asn
XM_011543690.1:c.1952C>A	XP_011541992.1:p.Thr651Asn
XM_017009986.1:c.1952C>A	XP_016865475.1:p.Thr651Asn
XR_002956185.1:n.3238C>A
NM_032380.5:c.1952C>A MANE Select	NP_115756.2:p.Thr651Asn
NM_001281302.2:c.2048C>A	NP_001268231.1:p.Thr683Asn
NM_170691.3:c.1811C>A	NP_733792.1:p.Thr604Asn
NR_104006.2:n.2017C>A