Canonical Allele Identifier: CA1400981636

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061938C= , CM000665.2:g.129061938C=	GRCh38
NC_000003.11:g.128780781C= , CM000665.1:g.128780781C=	GRCh37
NC_000003.10:g.130263471C=	NCBI36
NG_008715.1:g.6137C= , LRG_477:g.6137C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.199C= MANE Select	ENSP00000303942.4:p.Pro67=
ENST00000307395.4:c.199C=	ENSP00000303942.4:p.Pro67=
NM_000174.4:c.199C= , LRG_477t1:c.199C=	NP_000165.1:p.Pro67=
XM_005247374.3:c.199C=	XP_005247431.1:p.Pro67=
XM_011512701.1:c.199C=	XP_011511003.1:p.Pro67=
XM_011512702.1:c.199C=	XP_011511004.1:p.Pro67=
NM_000174.5:c.199C= MANE Select	NP_000165.1:p.Pro67=