Canonical Allele Identifier: CA1401004587
Gene: GP9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061653A= , CM000665.2:g.129061653A= GRCh38
NC_000003.11:g.128780496A= , CM000665.1:g.128780496A= GRCh37
NC_000003.10:g.130263186A= NCBI36
NG_008715.1:g.5852A= , LRG_477:g.5852A=

Transcript Alleles

HGVS Amino-acid change
ENST00000307395.5:c.-13+34A= MANE Select ENSP00000303942.4:n.-13+34A=
ENST00000307395.4:c.-13+34A= ENSP00000303942.4:n.-13+34A=
NM_000174.4:c.-13+34A= , LRG_477t1:c.-13+34A= NP_000165.1:n.-13+34A=
XM_005247374.3:c.-13+34A= XP_005247431.1:n.-13+34A=
XM_011512701.1:c.-13+34A= XP_011511003.1:n.-13+34A=
XM_011512702.1:c.-12-75A= XP_011511004.1:n.-12-75A=
NM_000174.5:c.-13+34A= MANE Select NP_000165.1:n.-13+34A=
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