Canonical Allele Identifier: CA443021103

Gene: TERT

Linked Data

• MyVariant Identifiers: chr5:g.1260627A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1260512A>G , CM000667.2:g.1260512A>G	GRCh38
NC_000005.9:g.1260627A>G , CM000667.1:g.1260627A>G	GRCh37
NC_000005.8:g.1313627A>G	NCBI36
NG_009265.1:g.39536T>C , LRG_343:g.39536T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2932T>C MANE Select	ENSP00000309572.5:p.Leu978=
ENST00000656021.1:c.*2478T>C	ENSP00000499759.1:n.*2478T>C
ENST00000667927.1:n.220T>C
ENST00000310581.9:c.2932T>C	ENSP00000309572.5:p.Leu978=
ENST00000334602.10:c.2743T>C	ENSP00000334346.6:p.Leu915=
ENST00000460137.6:c.2525T>C	ENSP00000425003.1:n.2525T>C
ENST00000484238.6:n.1374T>C
NM_001193376.1:c.2743T>C	NP_001180305.1:p.Leu915=
NM_198253.2:c.2932T>C , LRG_343t1:c.2932T>C	NP_937983.2:p.Leu978=
XM_011514104.1:c.1402T>C	XP_011512406.1:p.Leu468=
XM_011514105.1:c.1288T>C	XP_011512407.1:p.Leu430=
XM_011514106.1:c.1288T>C	XP_011512408.1:p.Leu430=
NR_149162.1:n.2619T>C
NR_149163.1:n.2583T>C
NM_001193376.2:c.2743T>C	NP_001180305.1:p.Leu915=
NM_198253.3:c.2932T>C MANE Select	NP_937983.2:p.Leu978=
NR_149162.2:n.2640T>C
NR_149163.2:n.2604T>C
NM_001193376.3:c.2743T>C	NP_001180305.1:p.Leu915=
NR_149162.3:n.2640T>C
NR_149163.3:n.2604T>C