Canonical Allele Identifier: CA1401004503

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061501C= , CM000665.2:g.129061501C=	GRCh38
NC_000003.11:g.128780344C= , CM000665.1:g.128780344C=	GRCh37
NC_000003.10:g.130263034C=	NCBI36
NG_008715.1:g.5700C= , LRG_477:g.5700C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-131C= MANE Select	ENSP00000303942.4:n.-131C=
ENST00000307395.4:c.-131C=	ENSP00000303942.4:n.-131C=
NM_000174.4:c.-131C= , LRG_477t1:c.-131C=	NP_000165.1:n.-131C=
XM_005247374.3:c.-131C=	XP_005247431.1:n.-131C=
XM_011512701.1:c.-131C=	XP_011511003.1:n.-131C=
XM_011512702.1:c.-12-227C=	XP_011511004.1:n.-12-227C=
NM_000174.5:c.-131C= MANE Select	NP_000165.1:n.-131C=