Canonical Allele Identifier: CA3502766

Gene: ARHGEF37

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149616754C>T , CM000667.2:g.149616754C>T	GRCh38
NC_000005.9:g.148996317C>T , CM000667.1:g.148996317C>T	GRCh37
NC_000005.8:g.148976510C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001001669.3:c.646C>T MANE Select	NP_001001669.2:p.Arg216Cys
ENST00000333677.7:c.646C>T MANE Select	ENSP00000328083.6:p.Arg216Cys
NM_001001669.2:c.646C>T	NP_001001669.2:p.Arg216Cys
ENST00000333677.6:c.646C>T	ENSP00000328083.6:p.Arg216Cys
XM_005268447.3:c.646C>T	XP_005268504.1:p.Arg216Cys
XM_005268447.4:c.646C>T	XP_005268504.1:p.Arg216Cys
XM_005268448.1:c.4C>T	XP_005268505.1:p.Arg2Cys
XM_006714784.2:c.646C>T	XP_006714847.1:p.Arg216Cys
XM_006714784.3:c.646C>T	XP_006714847.1:p.Arg216Cys
XM_011537642.1:c.679C>T	XP_011535944.1:p.Arg227Cys
XM_011537642.3:c.679C>T	XP_011535944.1:p.Arg227Cys
XM_011537643.1:c.679C>T	XP_011535945.1:p.Arg227Cys
XM_017009460.1:c.646C>T	XP_016864949.1:p.Arg216Cys
XM_017009461.2:c.4C>T	XP_016864950.1:p.Arg2Cys