Canonical Allele Identifier: CA1401004639
Gene: GP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061759T= , CM000665.2:g.129061759T= GRCh38
NC_000003.11:g.128780602T= , CM000665.1:g.128780602T= GRCh37
NC_000003.10:g.130263292T= NCBI36
NG_008715.1:g.5958T= , LRG_477:g.5958T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.20T= MANE Select ENSP00000303942.4:p.Leu7=
ENST00000307395.4:c.20T= ENSP00000303942.4:p.Leu7=
NM_000174.4:c.20T= , LRG_477t1:c.20T= NP_000165.1:p.Leu7=
XM_005247374.3:c.20T= XP_005247431.1:p.Leu7=
XM_011512701.1:c.20T= XP_011511003.1:p.Leu7=
XM_011512702.1:c.20T= XP_011511004.1:p.Leu7=
NM_000174.5:c.20T= MANE Select NP_000165.1:p.Leu7=