Canonical Allele Identifier: CA2579846034

Gene: TERT

Genomic Alleles

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

Transcript Alleles

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