Canonical Allele Identifier: CA359079633

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1278883A>C (hg19) ; chr5:g.1278768A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278768A>C , CM000667.2:g.1278768A>C	GRCh38
NC_000005.9:g.1278883A>C , CM000667.1:g.1278883A>C	GRCh37
NC_000005.8:g.1331883A>C	NCBI36
NG_009265.1:g.21280T>G , LRG_343:g.21280T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2159T>G MANE Select	ENSP00000309572.5:p.Ile720Ser
ENST00000656021.1:c.*1705T>G	ENSP00000499759.1:n.*1705T>G
ENST00000310581.9:c.2159T>G	ENSP00000309572.5:p.Ile720Ser
ENST00000334602.10:c.2159T>G	ENSP00000334346.6:p.Ile720Ser
ENST00000460137.6:c.2131-8T>G	ENSP00000425003.1:n.2131-8T>G
ENST00000484238.6:n.972T>G
ENST00000508104.2:c.2159T>G	ENSP00000426042.2:p.Ile720Ser
NM_001193376.1:c.2159T>G	NP_001180305.1:p.Ile720Ser
NM_198253.2:c.2159T>G , LRG_343t1:c.2159T>G	NP_937983.2:p.Ile720Ser
XM_011514104.1:c.629T>G	XP_011512406.1:p.Ile210Ser
XM_011514105.1:c.515T>G	XP_011512407.1:p.Ile172Ser
XM_011514106.1:c.515T>G	XP_011512408.1:p.Ile172Ser
NR_149162.1:n.2217T>G
NR_149163.1:n.2189-8T>G
NM_001193376.2:c.2159T>G	NP_001180305.1:p.Ile720Ser
NM_198253.3:c.2159T>G MANE Select	NP_937983.2:p.Ile720Ser
NR_149162.2:n.2238T>G
NR_149163.2:n.2210-8T>G
NM_001193376.3:c.2159T>G	NP_001180305.1:p.Ile720Ser
NR_149162.3:n.2238T>G
NR_149163.3:n.2210-8T>G