Canonical Allele Identifier: CA443021112

Gene: TERT

Linked Data

• gnomAD v4: 5-1260516-C-G
• MyVariant Identifiers: chr5:g.1260631C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260516C>G , CM000667.2:g.1260516C>G	GRCh38
NC_000005.9:g.1260631C>G , CM000667.1:g.1260631C>G	GRCh37
NC_000005.8:g.1313631C>G	NCBI36
NG_009265.1:g.39532G>C , LRG_343:g.39532G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2928G>C MANE Select	ENSP00000309572.5:p.Gly976=
ENST00000656021.1:c.*2474G>C	ENSP00000499759.1:n.*2474G>C
ENST00000667927.1:n.216G>C
ENST00000310581.9:c.2928G>C	ENSP00000309572.5:p.Gly976=
ENST00000334602.10:c.2739G>C	ENSP00000334346.6:p.Gly913=
ENST00000460137.6:c.2521G>C	ENSP00000425003.1:n.2521G>C
ENST00000484238.6:n.1370G>C
NM_001193376.1:c.2739G>C	NP_001180305.1:p.Gly913=
NM_198253.2:c.2928G>C , LRG_343t1:c.2928G>C	NP_937983.2:p.Gly976=
XM_011514104.1:c.1398G>C	XP_011512406.1:p.Gly466=
XM_011514105.1:c.1284G>C	XP_011512407.1:p.Gly428=
XM_011514106.1:c.1284G>C	XP_011512408.1:p.Gly428=
NR_149162.1:n.2615G>C
NR_149163.1:n.2579G>C
NM_001193376.2:c.2739G>C	NP_001180305.1:p.Gly913=
NM_198253.3:c.2928G>C MANE Select	NP_937983.2:p.Gly976=
NR_149162.2:n.2636G>C
NR_149163.2:n.2600G>C
NM_001193376.3:c.2739G>C	NP_001180305.1:p.Gly913=
NR_149162.3:n.2636G>C
NR_149163.3:n.2600G>C