Canonical Allele Identifier: CA1522533763

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1253629G= , CM000667.2:g.1253629G=	GRCh38
NC_000005.9:g.1253744G= , CM000667.1:g.1253744G=	GRCh37
NC_000005.8:g.1306744G=	NCBI36
NG_009265.1:g.46419C= , LRG_343:g.46419C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310581.10:c.*99C= MANE Select	ENSP00000309572.5:n.*99C=
ENST00000656021.1:c.*3044C=	ENSP00000499759.1:n.*3044C=
ENST00000310581.9:c.*99C=	ENSP00000309572.5:n.*99C=
ENST00000484238.6:n.1940C=
NM_001193376.1:c.*99C=	NP_001180305.1:n.*99C=
NM_198253.2:c.*99C= , LRG_343t1:c.*99C=	NP_937983.2:n.*99C=
XM_011514104.1:c.*99C=	XP_011512406.1:n.*99C=
XM_011514105.1:c.*99C=	XP_011512407.1:n.*99C=
XM_011514106.1:c.*99C=	XP_011512408.1:n.*99C=
XR_925683.1:n.287-1045G=
NR_149162.1:n.3185C=
NR_149163.1:n.3149C=
NM_001193376.2:c.*99C=	NP_001180305.1:n.*99C=
NM_198253.3:c.*99C= MANE Select	NP_937983.2:n.*99C=
NR_149162.2:n.3206C=
NR_149163.2:n.3170C=
NM_001193376.3:c.*99C=	NP_001180305.1:n.*99C=
NR_149162.3:n.3206C=
NR_149163.3:n.3170C=