Canonical Allele Identifier: CA360075965

Gene: GFM2

Linked Data

• MyVariant Identifiers: chr5:g.74021470G>A (hg19) ; chr5:g.74725645G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74725645G>A , CM000667.2:g.74725645G>A	GRCh38
NC_000005.9:g.74021470G>A , CM000667.1:g.74021470G>A	GRCh37
NC_000005.8:g.74057226G>A	NCBI36
NG_011531.1:g.46573C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2023C>T MANE Select	ENSP00000296805.3:p.Gln675Ter
ENST00000296805.7:c.2023C>T	ENSP00000296805.3:p.Gln675Ter
ENST00000345239.6:c.1882C>T	ENSP00000296804.3:p.Gln628Ter
ENST00000509430.5:c.2023C>T	ENSP00000427004.1:p.Gln675Ter
ENST00000515125.5:n.431+296C>T
NM_001281302.1:c.2119C>T	NP_001268231.1:p.Gln707Ter
NM_032380.4:c.2023C>T	NP_115756.2:p.Gln675Ter
NM_170691.2:c.1882C>T	NP_733792.1:p.Gln628Ter
NR_104006.1:n.2342C>T
XM_006714721.2:c.1888C>T	XP_006714784.1:p.Gln630Ter
XM_011543690.1:c.2023C>T	XP_011541992.1:p.Gln675Ter
XM_017009986.1:c.2023C>T	XP_016865475.1:p.Gln675Ter
XR_002956185.1:n.3309C>T
NM_032380.5:c.2023C>T MANE Select	NP_115756.2:p.Gln675Ter
NM_001281302.2:c.2119C>T	NP_001268231.1:p.Gln707Ter
NM_170691.3:c.1882C>T	NP_733792.1:p.Gln628Ter
NR_104006.2:n.2088C>T