Canonical Allele Identifier: CA359078792

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1278770C>G (hg19) ; chr5:g.1278655C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278655C>G , CM000667.2:g.1278655C>G	GRCh38
NC_000005.9:g.1278770C>G , CM000667.1:g.1278770C>G	GRCh37
NC_000005.8:g.1331770C>G	NCBI36
NG_009265.1:g.21393G>C , LRG_343:g.21393G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2272G>C MANE Select	ENSP00000309572.5:p.Ala758Pro
ENST00000656021.1:c.*1818G>C	ENSP00000499759.1:n.*1818G>C
ENST00000310581.9:c.2272G>C	ENSP00000309572.5:p.Ala758Pro
ENST00000334602.10:c.2272G>C	ENSP00000334346.6:p.Ala758Pro
ENST00000460137.6:c.2236G>C	ENSP00000425003.1:p.Ala746Pro
ENST00000484238.6:n.1085G>C
ENST00000508104.2:c.2272G>C	ENSP00000426042.2:p.Ala758Pro
NM_001193376.1:c.2272G>C	NP_001180305.1:p.Ala758Pro
NM_198253.2:c.2272G>C , LRG_343t1:c.2272G>C	NP_937983.2:p.Ala758Pro
XM_011514104.1:c.742G>C	XP_011512406.1:p.Ala248Pro
XM_011514105.1:c.628G>C	XP_011512407.1:p.Ala210Pro
XM_011514106.1:c.628G>C	XP_011512408.1:p.Ala210Pro
NR_149162.1:n.2330G>C
NR_149163.1:n.2294G>C
NM_001193376.2:c.2272G>C	NP_001180305.1:p.Ala758Pro
NM_198253.3:c.2272G>C MANE Select	NP_937983.2:p.Ala758Pro
NR_149162.2:n.2351G>C
NR_149163.2:n.2315G>C
NM_001193376.3:c.2272G>C	NP_001180305.1:p.Ala758Pro
NR_149162.3:n.2351G>C
NR_149163.3:n.2315G>C