Canonical Allele Identifier: CA4885918

Gene: TG

Linked Data

• ExAC: 8:134145907 AGCAAAGCCCTGGGACAAGTGGAGGGAGCTGGGTGTTGATCTCAGCATCTGCTGTGCTCGCTGCATGAGACCTGTGCTGCGCGCGCAT / A
• gnomAD v2: 8-134145907-AGCAAAGCCCTGGGACAAGTGGAGGGAGCTGGGTGTTGATCTCAGCATCTGCTGTGCTCGCTGCATGAGACCTGTGCTGCGCGCGCAT-A
• gnomAD v4: 8-133133663-AGCAAAGCCCTGGGACAAGTGGAGGGAGCTGGGTGTTGATCTCAGCATCTGCTGTGCTCGCTGCATGAGACCTGTGCTGCGCGCGCAT-A
• MyVariant Identifiers: chr8:g.134145908_134145994del (hg19) ; chr8:g.133133664_133133750del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133664_133133750del , CM000670.2:g.133133664_133133750del	GRCh38
NC_000008.10:g.134145908_134145994del , CM000670.1:g.134145908_134145994del	GRCh37
NC_000008.9:g.134215090_134215176del	NCBI36
NG_015832.1:g.271704_271790del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8188+4_8188+90del MANE Select	ENSP00000220616.4:n.8188+4_8188+90del
ENST00000220616.8:c.8188+4_8188+90del	ENSP00000220616.4:n.8188+4_8188+90del
ENST00000519178.5:c.3554+4_3554+90del
ENST00000519543.5:c.2587+4_2587+90del	ENSP00000430430.1:n.2587+4_2587+90del
ENST00000521107.1:c.400+4_400+90del	ENSP00000430161.1:n.400+4_400+90del
ENST00000522691.1:n.274+4_274+90del
ENST00000523756.5:c.4843+4_4843+90del
NM_003235.4:c.8188+4_8188+90del	NP_003226.4:n.8188+4_8188+90del
XM_005251038.3:c.7996+4_7996+90del	XP_005251095.1:n.7996+4_7996+90del
XM_006716622.2:c.8125+4_8125+90del	XP_006716685.1:n.8125+4_8125+90del
XM_005251038.4:c.7996+4_7996+90del	XP_005251095.1:n.7996+4_7996+90del
XM_006716622.3:c.8125+4_8125+90del	XP_006716685.1:n.8125+4_8125+90del
XM_017013793.1:c.8122+4_8122+90del	XP_016869282.1:n.8122+4_8122+90del
XM_017013794.1:c.8053+4_8053+90del	XP_016869283.1:n.8053+4_8053+90del
XM_017013795.1:c.8017+4_8017+90del	XP_016869284.1:n.8017+4_8017+90del
XM_017013796.1:c.7969+4_7969+90del	XP_016869285.1:n.7969+4_7969+90del
XM_017013797.1:c.7927+4_7927+90del	XP_016869286.1:n.7927+4_7927+90del
NM_003235.5:c.8188+4_8188+90del MANE Select	NP_003226.4:n.8188+4_8188+90del