Canonical Allele Identifier: CA372252945

Gene: TG

Linked Data

• ClinVar Variation Id: 3006088
• ClinVar RCV Id: RCV003866239
• dbSNP Id: rs1289334451
• gnomAD v2: 8-134145690-ATTTC-A
• gnomAD v3: 8-133133446-ATTTC-A
• gnomAD v4: 8-133133446-ATTTC-A
• MyVariant Identifiers: chr8:g.134145691_134145694del (hg19) ; chr8:g.133133448_133133451del (hg38) ; chr8:g.133133447_133133450del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133453_133133456del , CM000670.2:g.133133453_133133456del	GRCh38
NC_000008.10:g.134145697_134145700del , CM000670.1:g.134145697_134145700del	GRCh37
NC_000008.9:g.134214879_134214882del	NCBI36
NG_015832.1:g.271493_271496del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7998-17_7998-14del MANE Select	ENSP00000220616.4:n.7998-17_7998-14del
ENST00000220616.8:c.7998-17_7998-14del	ENSP00000220616.4:n.7998-17_7998-14del
ENST00000519178.5:c.3364-17_3364-14del
ENST00000519543.5:c.2397-17_2397-14del	ENSP00000430430.1:n.2397-17_2397-14del
ENST00000521107.1:c.210-17_210-14del	ENSP00000430161.1:n.210-17_210-14del
ENST00000522691.1:n.67_70del
ENST00000523756.5:c.4653-17_4653-14del
NM_003235.4:c.7998-17_7998-14del	NP_003226.4:n.7998-17_7998-14del
XM_005251038.3:c.7806-17_7806-14del	XP_005251095.1:n.7806-17_7806-14del
XM_006716622.2:c.7935-17_7935-14del	XP_006716685.1:n.7935-17_7935-14del
XM_005251038.4:c.7806-17_7806-14del	XP_005251095.1:n.7806-17_7806-14del
XM_006716622.3:c.7935-17_7935-14del	XP_006716685.1:n.7935-17_7935-14del
XM_017013793.1:c.7932-17_7932-14del	XP_016869282.1:n.7932-17_7932-14del
XM_017013794.1:c.7863-17_7863-14del	XP_016869283.1:n.7863-17_7863-14del
XM_017013795.1:c.7827-17_7827-14del	XP_016869284.1:n.7827-17_7827-14del
XM_017013796.1:c.7779-17_7779-14del	XP_016869285.1:n.7779-17_7779-14del
XM_017013797.1:c.7737-17_7737-14del	XP_016869286.1:n.7737-17_7737-14del
NM_003235.5:c.7998-17_7998-14del MANE Select	NP_003226.4:n.7998-17_7998-14del