Canonical Allele Identifier: CA359073217

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1266615A>G (hg19) ; chr5:g.1266500A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1266500A>G , CM000667.2:g.1266500A>G	GRCh38
NC_000005.9:g.1266615A>G , CM000667.1:g.1266615A>G	GRCh37
NC_000005.8:g.1319615A>G	NCBI36
NG_009265.1:g.33548T>C , LRG_343:g.33548T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2618T>C MANE Select	ENSP00000309572.5:p.Val873Ala
ENST00000656021.1:c.*2164T>C	ENSP00000499759.1:n.*2164T>C
ENST00000310581.9:c.2618T>C	ENSP00000309572.5:p.Val873Ala
ENST00000334602.10:c.2618T>C	ENSP00000334346.6:p.Val873Ala
ENST00000460137.6:c.2400T>C	ENSP00000425003.1:n.2400T>C
ENST00000484238.6:n.1249T>C
ENST00000503656.1:n.25T>C
ENST00000508104.2:c.2436T>C	ENSP00000426042.2:n.2436T>C
NM_001193376.1:c.2618T>C	NP_001180305.1:p.Val873Ala
NM_198253.2:c.2618T>C , LRG_343t1:c.2618T>C	NP_937983.2:p.Val873Ala
XM_011514104.1:c.1088T>C	XP_011512406.1:p.Val363Ala
XM_011514105.1:c.974T>C	XP_011512407.1:p.Val325Ala
XM_011514106.1:c.974T>C	XP_011512408.1:p.Val325Ala
NR_149162.1:n.2494T>C
NR_149163.1:n.2458T>C
NM_001193376.2:c.2618T>C	NP_001180305.1:p.Val873Ala
NM_198253.3:c.2618T>C MANE Select	NP_937983.2:p.Val873Ala
NR_149162.2:n.2515T>C
NR_149163.2:n.2479T>C
NM_001193376.3:c.2618T>C	NP_001180305.1:p.Val873Ala
NR_149162.3:n.2515T>C
NR_149163.3:n.2479T>C