Canonical Allele Identifier: CA2579846037

Gene: TERT

Linked Data

• gnomAD v4: 5-1295045-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1295045C>T , CM000667.2:g.1295045C>T	GRCh38
NC_000005.9:g.1295160C>T , CM000667.1:g.1295160C>T	GRCh37
NC_000005.8:g.1348160C>T	NCBI36
NG_009265.1:g.5003G>A , LRG_343:g.5003G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.-56G>A MANE Select	ENSP00000309572.5:n.-56G>A
ENST00000656021.1:c.-56G>A	ENSP00000499759.1:n.-56G>A
ENST00000310581.9:c.-56G>A	ENSP00000309572.5:n.-56G>A
ENST00000522877.1:n.25G>A
NM_001193376.1:c.-56G>A	NP_001180305.1:n.-56G>A
NM_198253.2:c.-56G>A , LRG_343t1:c.-56G>A	NP_937983.2:n.-56G>A
NR_149162.1:n.3G>A
NR_149163.1:n.3G>A
NM_001193376.2:c.-56G>A	NP_001180305.1:n.-56G>A
NM_198253.3:c.-56G>A MANE Select	NP_937983.2:n.-56G>A
NR_149162.2:n.24G>A
NR_149163.2:n.24G>A
NM_001193376.3:c.-56G>A	NP_001180305.1:n.-56G>A
NR_149162.3:n.24G>A
NR_149163.3:n.24G>A