Canonical Allele Identifier: CA354447196
Gene: GP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061908C>G , CM000665.2:g.129061908C>G GRCh38
NC_000003.11:g.128780751C>G , CM000665.1:g.128780751C>G GRCh37
NC_000003.10:g.130263441C>G NCBI36
NG_008715.1:g.6107C>G , LRG_477:g.6107C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.169C>G MANE Select ENSP00000303942.4:p.Leu57Val
ENST00000307395.4:c.169C>G ENSP00000303942.4:p.Leu57Val
NM_000174.4:c.169C>G , LRG_477t1:c.169C>G NP_000165.1:p.Leu57Val
XM_005247374.3:c.169C>G XP_005247431.1:p.Leu57Val
XM_011512701.1:c.169C>G XP_011511003.1:p.Leu57Val
XM_011512702.1:c.169C>G XP_011511004.1:p.Leu57Val
NM_000174.5:c.169C>G MANE Select NP_000165.1:p.Leu57Val