Canonical Allele Identifier: CA1401004548
Gene: GP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061590_129061593delinsAGAG , CM000665.2:g.129061590_129061593delinsAGAG GRCh38
NC_000003.11:g.128780433_128780436delinsAGAG , CM000665.1:g.128780433_128780436delinsAGAG GRCh37
NC_000003.10:g.130263123_130263126delinsAGAG NCBI36
NG_008715.1:g.5789_5792delinsAGAG , LRG_477:g.5789_5792delinsAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-42_-39delinsAGAG MANE Select ENSP00000303942.4:n.-42_-39delinsAGAG
ENST00000307395.4:c.-42_-39delinsAGAG ENSP00000303942.4:n.-42_-39delinsAGAG
NM_000174.4:c.-42_-39delinsAGAG , LRG_477t1:c.-42_-39delinsAGAG NP_000165.1:n.-42_-39delinsAGAG
XM_005247374.3:c.-42_-39delinsAGAG XP_005247431.1:n.-42_-39delinsAGAG
XM_011512701.1:c.-42_-39delinsAGAG XP_011511003.1:n.-42_-39delinsAGAG
XM_011512702.1:c.-12-138_-12-135delinsAGAG XP_011511004.1:n.-12-138_-12-135delinsAGAG
NM_000174.5:c.-42_-39delinsAGAG MANE Select NP_000165.1:n.-42_-39delinsAGAG