Canonical Allele Identifier: CA359069702

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1260609T>A (hg19) ; chr5:g.1260494T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260494T>A , CM000667.2:g.1260494T>A	GRCh38
NC_000005.9:g.1260609T>A , CM000667.1:g.1260609T>A	GRCh37
NC_000005.8:g.1313609T>A	NCBI36
NG_009265.1:g.39554A>T , LRG_343:g.39554A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.2950A>T MANE Select	ENSP00000309572.5:p.Ser984Cys
ENST00000656021.1:c.*2496A>T	ENSP00000499759.1:n.*2496A>T
ENST00000667927.1:n.238A>T
ENST00000310581.9:c.2950A>T	ENSP00000309572.5:p.Ser984Cys
ENST00000334602.10:c.2761A>T	ENSP00000334346.6:p.Ser921Cys
ENST00000460137.6:c.2543A>T	ENSP00000425003.1:n.2543A>T
ENST00000484238.6:n.1392A>T
NM_001193376.1:c.2761A>T	NP_001180305.1:p.Ser921Cys
NM_198253.2:c.2950A>T , LRG_343t1:c.2950A>T	NP_937983.2:p.Ser984Cys
XM_011514104.1:c.1420A>T	XP_011512406.1:p.Ser474Cys
XM_011514105.1:c.1306A>T	XP_011512407.1:p.Ser436Cys
XM_011514106.1:c.1306A>T	XP_011512408.1:p.Ser436Cys
NR_149162.1:n.2637A>T
NR_149163.1:n.2601A>T
NM_001193376.2:c.2761A>T	NP_001180305.1:p.Ser921Cys
NM_198253.3:c.2950A>T MANE Select	NP_937983.2:p.Ser984Cys
NR_149162.2:n.2658A>T
NR_149163.2:n.2622A>T
NM_001193376.3:c.2761A>T	NP_001180305.1:p.Ser921Cys
NR_149162.3:n.2658A>T
NR_149163.3:n.2622A>T