Canonical Allele Identifier: CA2579846018
Gene: TERT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1295036C>G , CM000667.2:g.1295036C>G GRCh38
NC_000005.9:g.1295151C>G , CM000667.1:g.1295151C>G GRCh37
NC_000005.8:g.1348151C>G NCBI36
NG_009265.1:g.5012G>C , LRG_343:g.5012G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000310581.10:c.-47G>C MANE Select ENSP00000309572.5:n.-47G>C
ENST00000656021.1:c.-47G>C ENSP00000499759.1:n.-47G>C
ENST00000310581.9:c.-47G>C ENSP00000309572.5:n.-47G>C
ENST00000522877.1:n.34G>C
NM_001193376.1:c.-47G>C NP_001180305.1:n.-47G>C
NM_198253.2:c.-47G>C , LRG_343t1:c.-47G>C NP_937983.2:n.-47G>C
NR_149162.1:n.12G>C
NR_149163.1:n.12G>C
NM_001193376.2:c.-47G>C NP_001180305.1:n.-47G>C
NM_198253.3:c.-47G>C MANE Select NP_937983.2:n.-47G>C
NR_149162.2:n.33G>C
NR_149163.2:n.33G>C
NM_001193376.3:c.-47G>C NP_001180305.1:n.-47G>C
NR_149162.3:n.33G>C
NR_149163.3:n.33G>C