Canonical Allele Identifier: CA444851913

Gene: GFM2

Linked Data

• MyVariant Identifiers: chr5:g.74021561T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74725736T>C , CM000667.2:g.74725736T>C	GRCh38
NC_000005.9:g.74021561T>C , CM000667.1:g.74021561T>C	GRCh37
NC_000005.8:g.74057317T>C	NCBI36
NG_011531.1:g.46482A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.1932A>G MANE Select	ENSP00000296805.3:p.Pro644=
ENST00000296805.7:c.1932A>G	ENSP00000296805.3:p.Pro644=
ENST00000345239.6:c.1791A>G	ENSP00000296804.3:p.Pro597=
ENST00000509430.5:c.1932A>G	ENSP00000427004.1:p.Pro644=
ENST00000514734.5:n.843A>G
ENST00000515125.5:n.431+205A>G
NM_001281302.1:c.2028A>G	NP_001268231.1:p.Pro676=
NM_032380.4:c.1932A>G	NP_115756.2:p.Pro644=
NM_170691.2:c.1791A>G	NP_733792.1:p.Pro597=
NR_104006.1:n.2251A>G
XM_006714721.2:c.1797A>G	XP_006714784.1:p.Pro599=
XM_011543690.1:c.1932A>G	XP_011541992.1:p.Pro644=
XM_017009986.1:c.1932A>G	XP_016865475.1:p.Pro644=
XR_002956185.1:n.3218A>G
NM_032380.5:c.1932A>G MANE Select	NP_115756.2:p.Pro644=
NM_001281302.2:c.2028A>G	NP_001268231.1:p.Pro676=
NM_170691.3:c.1791A>G	NP_733792.1:p.Pro597=
NR_104006.2:n.1997A>G