Canonical Allele Identifier: CA557858704

Gene: TERT

Linked Data

• gnomAD v2: 5-1295152-A-ACCACACTGGGATCCG
• gnomAD v4: 5-1295037-A-ACCACACTGGGATCCG
• MyVariant Identifiers: chr5:g.1295152_1295153insCCACACTGGGATCCG (hg19) ; chr5:g.1295037_1295038insCCACACTGGGATCCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1295037_1295038insCCACACTGGGATCCG , CM000667.2:g.1295037_1295038insCCACACTGGGATCCG	GRCh38
NC_000005.9:g.1295152_1295153insCCACACTGGGATCCG , CM000667.1:g.1295152_1295153insCCACACTGGGATCCG	GRCh37
NC_000005.8:g.1348152_1348153insCCACACTGGGATCCG	NCBI36
NG_009265.1:g.5010_5011insCGGATCCCAGTGTGG , LRG_343:g.5010_5011insCGGATCCCAGTGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.-49_-48insCGGATCCCAGTGTGG MANE Select	ENSP00000309572.5:n.-49_-48insCGGATCCCAGTGTGG
ENST00000656021.1:c.-49_-48insCGGATCCCAGTGTGG	ENSP00000499759.1:n.-49_-48insCGGATCCCAGTGTGG
ENST00000310581.9:c.-49_-48insCGGATCCCAGTGTGG	ENSP00000309572.5:n.-49_-48insCGGATCCCAGTGTGG
ENST00000522877.1:n.32_33insCGGATCCCAGTGTGG
NM_001193376.1:c.-49_-48insCGGATCCCAGTGTGG	NP_001180305.1:n.-49_-48insCGGATCCCAGTGTGG
NM_198253.2:c.-49_-48insCGGATCCCAGTGTGG , LRG_343t1:c.-49_-48insCGGATCCCAGTGTGG	NP_937983.2:n.-49_-48insCGGATCCCAGTGTGG
NR_149162.1:n.10_11insCGGATCCCAGTGTGG
NR_149163.1:n.10_11insCGGATCCCAGTGTGG
NM_001193376.2:c.-49_-48insCGGATCCCAGTGTGG	NP_001180305.1:n.-49_-48insCGGATCCCAGTGTGG
NM_198253.3:c.-49_-48insCGGATCCCAGTGTGG MANE Select	NP_937983.2:n.-49_-48insCGGATCCCAGTGTGG
NR_149162.2:n.31_32insCGGATCCCAGTGTGG
NR_149163.2:n.31_32insCGGATCCCAGTGTGG
NM_001193376.3:c.-49_-48insCGGATCCCAGTGTGG	NP_001180305.1:n.-49_-48insCGGATCCCAGTGTGG
NR_149162.3:n.31_32insCGGATCCCAGTGTGG
NR_149163.3:n.31_32insCGGATCCCAGTGTGG