Canonical Allele Identifier: CA1401004588
Gene: GP9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061658C= , CM000665.2:g.129061658C= GRCh38
NC_000003.11:g.128780501C= , CM000665.1:g.128780501C= GRCh37
NC_000003.10:g.130263191C= NCBI36
NG_008715.1:g.5857C= , LRG_477:g.5857C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-13+39C= MANE Select ENSP00000303942.4:n.-13+39C=
ENST00000307395.4:c.-13+39C= ENSP00000303942.4:n.-13+39C=
NM_000174.4:c.-13+39C= , LRG_477t1:c.-13+39C= NP_000165.1:n.-13+39C=
XM_005247374.3:c.-13+39C= XP_005247431.1:n.-13+39C=
XM_011512701.1:c.-13+39C= XP_011511003.1:n.-13+39C=
XM_011512702.1:c.-12-70C= XP_011511004.1:n.-12-70C=
NM_000174.5:c.-13+39C= MANE Select NP_000165.1:n.-13+39C=
Search 100 bp 5'
Search 100 bp 3'