Canonical Allele Identifier: CA3184583

Gene: TERT

Linked Data

• dbSNP Id: rs767797406
• ExAC: 5:1272398 G / GGCTCTTGAAGGCCTTGCGGA
• gnomAD v4: 5-1272283-G-GGCTCTTGAAGGCCTTGCGGA
• MyVariant Identifiers: chr5:g.1272398_1272399insGCTCTTGAAGGCCTTGCGGA (hg19) ; chr5:g.1272283_1272284insGCTCTTGAAGGCCTTGCGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1272283_1272284insGCTCTTGAAGGCCTTGCGGA , CM000667.2:g.1272283_1272284insGCTCTTGAAGGCCTTGCGGA	GRCh38
NC_000005.9:g.1272398_1272399insGCTCTTGAAGGCCTTGCGGA , CM000667.1:g.1272398_1272399insGCTCTTGAAGGCCTTGCGGA	GRCh37
NC_000005.8:g.1325398_1325399insGCTCTTGAAGGCCTTGCGGA	NCBI36
NG_009265.1:g.27764_27765insTCCGCAAGGCCTTCAAGAGC , LRG_343:g.27764_27765insTCCGCAAGGCCTTCAAGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC MANE Select	ENSP00000309572.5:n.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC
ENST00000656021.1:c.*1833-4_*1833-3insTCCGCAAGGCCTTCAAGAGC	ENSP00000499759.1:n.*1833-4_*1833-3insTCCGCAAGGCCTTCAAGAGC
ENST00000310581.9:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC	ENSP00000309572.5:n.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC
ENST00000334602.10:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC	ENSP00000334346.6:n.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC
ENST00000460137.6:c.2251-3651_2251-3650insTCCGCAAGGCCTTCAAGAGC	ENSP00000425003.1:n.2251-3651_2251-3650insTCCGCAAGGCCTTCAAGAG...
ENST00000484238.6:n.1100-3651_1100-3650insTCCGCAAGGCCTTCAAGAGC
ENST00000508104.2:c.2287-3651_2287-3650insTCCGCAAGGCCTTCAAGAGC	ENSP00000426042.2:n.2287-3651_2287-3650insTCCGCAAGGCCTTCAAGAG...
NM_001193376.1:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC	NP_001180305.1:n.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC
NM_198253.2:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC , LRG_343t1:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC	NP_937983.2:n.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC
XM_011514104.1:c.757-4_757-3insTCCGCAAGGCCTTCAAGAGC	XP_011512406.1:n.757-4_757-3insTCCGCAAGGCCTTCAAGAGC
XM_011514105.1:c.643-4_643-3insTCCGCAAGGCCTTCAAGAGC	XP_011512407.1:n.643-4_643-3insTCCGCAAGGCCTTCAAGAGC
XM_011514106.1:c.643-4_643-3insTCCGCAAGGCCTTCAAGAGC	XP_011512408.1:n.643-4_643-3insTCCGCAAGGCCTTCAAGAGC
NR_149162.1:n.2345-3651_2345-3650insTCCGCAAGGCCTTCAAGAGC
NR_149163.1:n.2309-3651_2309-3650insTCCGCAAGGCCTTCAAGAGC
NM_001193376.2:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC	NP_001180305.1:n.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC
NM_198253.3:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC MANE Select	NP_937983.2:n.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC
NR_149162.2:n.2366-3651_2366-3650insTCCGCAAGGCCTTCAAGAGC
NR_149163.2:n.2330-3651_2330-3650insTCCGCAAGGCCTTCAAGAGC
NM_001193376.3:c.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC	NP_001180305.1:n.2287-4_2287-3insTCCGCAAGGCCTTCAAGAGC
NR_149162.3:n.2366-3651_2366-3650insTCCGCAAGGCCTTCAAGAGC
NR_149163.3:n.2330-3651_2330-3650insTCCGCAAGGCCTTCAAGAGC