Canonical Allele Identifier: CA2579846032

Gene: TERT

Linked Data

• dbSNP Id: rs2126693656
• gnomAD v4: 5-1295043-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1295043G>C , CM000667.2:g.1295043G>C	GRCh38
NC_000005.9:g.1295158G>C , CM000667.1:g.1295158G>C	GRCh37
NC_000005.8:g.1348158G>C	NCBI36
NG_009265.1:g.5005C>G , LRG_343:g.5005C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.-54C>G MANE Select	ENSP00000309572.5:n.-54C>G
ENST00000656021.1:c.-54C>G	ENSP00000499759.1:n.-54C>G
ENST00000310581.9:c.-54C>G	ENSP00000309572.5:n.-54C>G
ENST00000522877.1:n.27C>G
NM_001193376.1:c.-54C>G	NP_001180305.1:n.-54C>G
NM_198253.2:c.-54C>G , LRG_343t1:c.-54C>G	NP_937983.2:n.-54C>G
NR_149162.1:n.5C>G
NR_149163.1:n.5C>G
NM_001193376.2:c.-54C>G	NP_001180305.1:n.-54C>G
NM_198253.3:c.-54C>G MANE Select	NP_937983.2:n.-54C>G
NR_149162.2:n.26C>G
NR_149163.2:n.26C>G
NM_001193376.3:c.-54C>G	NP_001180305.1:n.-54C>G
NR_149162.3:n.26C>G
NR_149163.3:n.26C>G