Canonical Allele Identifier: CA649597556

Gene: TERT

Linked Data

• COSMIC: COSN1307006

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1295045_1295046insG , CM000667.2:g.1295045_1295046insG	GRCh38
NC_000005.9:g.1295160_1295161insG , CM000667.1:g.1295160_1295161insG	GRCh37
NC_000005.8:g.1348160_1348161insG	NCBI36
NG_009265.1:g.5002_5003insC , LRG_343:g.5002_5003insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.-57_-56insC MANE Select	ENSP00000309572.5:n.-57_-56insC
ENST00000656021.1:c.-57_-56insC	ENSP00000499759.1:n.-57_-56insC
ENST00000310581.9:c.-57_-56insC	ENSP00000309572.5:n.-57_-56insC
ENST00000522877.1:n.24_25insC
NM_001193376.1:c.-57_-56insC	NP_001180305.1:n.-57_-56insC
NM_198253.2:c.-57_-56insC , LRG_343t1:c.-57_-56insC	NP_937983.2:n.-57_-56insC
NR_149162.1:n.2_3insC
NR_149163.1:n.2_3insC
NM_001193376.2:c.-57_-56insC	NP_001180305.1:n.-57_-56insC
NM_198253.3:c.-57_-56insC MANE Select	NP_937983.2:n.-57_-56insC
NR_149162.2:n.23_24insC
NR_149163.2:n.23_24insC
NM_001193376.3:c.-57_-56insC	NP_001180305.1:n.-57_-56insC
NR_149162.3:n.23_24insC
NR_149163.3:n.23_24insC