Canonical Allele Identifier: CA1401004485
Gene: GP9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061463C= , CM000665.2:g.129061463C= GRCh38
NC_000003.11:g.128780306C= , CM000665.1:g.128780306C= GRCh37
NC_000003.10:g.130262996C= NCBI36
NG_008715.1:g.5662C= , LRG_477:g.5662C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-138-31C= MANE Select ENSP00000303942.4:n.-138-31C=
ENST00000307395.4:c.-138-31C= ENSP00000303942.4:n.-138-31C=
NM_000174.4:c.-138-31C= , LRG_477t1:c.-138-31C= NP_000165.1:n.-138-31C=
XM_005247374.3:c.-138-31C= XP_005247431.1:n.-138-31C=
XM_011512701.1:c.-138-31C= XP_011511003.1:n.-138-31C=
XM_011512702.1:c.-12-265C= XP_011511004.1:n.-12-265C=
NM_000174.5:c.-138-31C= MANE Select NP_000165.1:n.-138-31C=
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