Canonical Allele Identifier: CA359068014

Gene: TERT

Linked Data

• COSMIC: COSM3849762 ; COSM3849763
• MyVariant Identifiers: chr5:g.1255409C>A (hg19) ; chr5:g.1255294C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1255294C>A , CM000667.2:g.1255294C>A	GRCh38
NC_000005.9:g.1255409C>A , CM000667.1:g.1255409C>A	GRCh37
NC_000005.8:g.1308409C>A	NCBI36
NG_009265.1:g.44754G>T , LRG_343:g.44754G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.3150G>T MANE Select	ENSP00000309572.5:p.Lys1050Asn
ENST00000656021.1:c.*2696G>T	ENSP00000499759.1:n.*2696G>T
ENST00000667927.1:n.438G>T
ENST00000310581.9:c.3150G>T	ENSP00000309572.5:p.Lys1050Asn
ENST00000334602.10:c.2961G>T	ENSP00000334346.6:p.Lys987Asn
ENST00000460137.6:c.2743G>T	ENSP00000425003.1:n.2743G>T
ENST00000484238.6:n.1592G>T
NM_001193376.1:c.2961G>T	NP_001180305.1:p.Lys987Asn
NM_198253.2:c.3150G>T , LRG_343t1:c.3150G>T	NP_937983.2:p.Lys1050Asn
XM_011514104.1:c.1620G>T	XP_011512406.1:p.Lys540Asn
XM_011514105.1:c.1506G>T	XP_011512407.1:p.Lys502Asn
XM_011514106.1:c.1506G>T	XP_011512408.1:p.Lys502Asn
XR_925683.1:n.347-12C>A
NR_149162.1:n.2837G>T
NR_149163.1:n.2801G>T
NM_001193376.2:c.2961G>T	NP_001180305.1:p.Lys987Asn
NM_198253.3:c.3150G>T MANE Select	NP_937983.2:p.Lys1050Asn
NR_149162.2:n.2858G>T
NR_149163.2:n.2822G>T
NM_001193376.3:c.2961G>T	NP_001180305.1:p.Lys987Asn
NR_149162.3:n.2858G>T
NR_149163.3:n.2822G>T