Canonical Allele Identifier: CA354446460

Gene: GP9

Linked Data

• COSMIC: COSM215890
• MyVariant Identifiers: chr3:g.128780628G>T (hg19) ; chr3:g.129061785G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061785G>T , CM000665.2:g.129061785G>T	GRCh38
NC_000003.11:g.128780628G>T , CM000665.1:g.128780628G>T	GRCh37
NC_000003.10:g.130263318G>T	NCBI36
NG_008715.1:g.5984G>T , LRG_477:g.5984G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.46G>T MANE Select	ENSP00000303942.4:p.Ala16Ser
ENST00000307395.4:c.46G>T	ENSP00000303942.4:p.Ala16Ser
NM_000174.4:c.46G>T , LRG_477t1:c.46G>T	NP_000165.1:p.Ala16Ser
XM_005247374.3:c.46G>T	XP_005247431.1:p.Ala16Ser
XM_011512701.1:c.46G>T	XP_011511003.1:p.Ala16Ser
XM_011512702.1:c.46G>T	XP_011511004.1:p.Ala16Ser
NM_000174.5:c.46G>T MANE Select	NP_000165.1:p.Ala16Ser