Canonical Allele Identifier: CA1401004482

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061444G= , CM000665.2:g.129061444G=	GRCh38
NC_000003.11:g.128780287G= , CM000665.1:g.128780287G=	GRCh37
NC_000003.10:g.130262977G=	NCBI36
NG_008715.1:g.5643G= , LRG_477:g.5643G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-138-50G= MANE Select	ENSP00000303942.4:n.-138-50G=
ENST00000307395.4:c.-138-50G=	ENSP00000303942.4:n.-138-50G=
NM_000174.4:c.-138-50G= , LRG_477t1:c.-138-50G=	NP_000165.1:n.-138-50G=
XM_005247374.3:c.-138-50G=	XP_005247431.1:n.-138-50G=
XM_011512701.1:c.-138-50G=	XP_011511003.1:n.-138-50G=
XM_011512702.1:c.-12-284G=	XP_011511004.1:n.-12-284G=
NM_000174.5:c.-138-50G= MANE Select	NP_000165.1:n.-138-50G=