Canonical Allele Identifier: CA3408120

Gene: GDF9

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132861601G>A , CM000667.2:g.132861601G>A	GRCh38
NC_000005.9:g.132197293G>A , CM000667.1:g.132197293G>A	GRCh37
NC_000005.8:g.132225192G>A	NCBI36
NG_047051.1:g.10284C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296875.4:c.1089C>T	ENSP00000296875.3:p.Cys363=
ENST00000464378.2:c.1353C>T	ENSP00000509893.1:p.Cys451=
ENST00000621295.5:c.1089C>T	ENSP00000484339.1:p.Cys363=
ENST00000624492.4:c.1089C>T	ENSP00000485037.1:p.Cys363=
ENST00000624495.4:c.1089C>T	ENSP00000485231.1:p.Cys363=
ENST00000687138.1:c.1353C>T MANE Select	ENSP00000510441.1:p.Cys451=
ENST00000687214.1:c.1068C>T	ENSP00000509237.1:p.Cys356=
ENST00000296875.3:c.1089C>T	ENSP00000296875.3:p.Cys363=
ENST00000378673.2:c.1353C>T	ENSP00000367942.2:p.Cys451=
ENST00000621295.4:c.1089C>T	ENSP00000484339.1:p.Cys363=
ENST00000624492.3:c.1089C>T	ENSP00000485037.1:p.Cys363=
ENST00000624495.3:c.1089C>T	ENSP00000485231.1:p.Cys363=
NM_001288824.2:c.1089C>T	NP_001275753.1:p.Cys363=
NM_001288825.2:c.1089C>T	NP_001275754.1:p.Cys363=
NM_001288826.2:c.1089C>T	NP_001275755.1:p.Cys363=
NM_001288827.2:c.1089C>T	NP_001275756.1:p.Cys363=
NM_001288828.2:c.1089C>T	NP_001275757.1:p.Cys363=
NM_005260.4:c.1353C>T	NP_005251.1:p.Cys451=
XM_005271957.3:c.1089C>T	XP_005272014.1:p.Cys363=
XM_006714585.2:c.1089C>T	XP_006714648.1:p.Cys363=
XM_011543308.1:c.1353C>T	XP_011541610.1:p.Cys451=
XM_011543309.1:c.1089C>T	XP_011541611.1:p.Cys363=
XM_011543310.1:c.1089C>T	XP_011541612.1:p.Cys363=
XM_011543311.1:c.819C>T	XP_011541613.1:p.Cys273=
NM_005260.5:c.1353C>T	NP_005251.1:p.Cys451=
XM_005271957.5:c.1089C>T	XP_005272014.1:p.Cys363=
XM_006714585.4:c.1089C>T	XP_006714648.1:p.Cys363=
XM_011543308.3:c.1353C>T	XP_011541610.1:p.Cys451=
XM_011543311.3:c.819C>T	XP_011541613.1:p.Cys273=
NM_001288824.4:c.1089C>T	NP_001275753.1:p.Cys363=
NM_001288825.4:c.1089C>T	NP_001275754.1:p.Cys363=
NM_001288826.3:c.1089C>T	NP_001275755.1:p.Cys363=
NM_001288827.3:c.1089C>T	NP_001275756.1:p.Cys363=
NM_001288828.3:c.1089C>T	NP_001275757.1:p.Cys363=
NM_005260.7:c.1353C>T MANE Select	NP_005251.1:p.Cys451=