Canonical Allele Identifier: CA557563006

Gene: TERT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1254510G>A , CM000667.2:g.1254510G>A	GRCh38
NC_000005.9:g.1254625G>A , CM000667.1:g.1254625G>A	GRCh37
NC_000005.8:g.1307625G>A	NCBI36
NG_009265.1:g.45538C>T , LRG_343:g.45538C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_198253.3:c.3158-5C>T MANE Select	NP_937983.2:n.3158-5C>T
ENST00000310581.10:c.3158-5C>T MANE Select	ENSP00000309572.5:n.3158-5C>T
NM_001193376.1:c.2969-5C>T	NP_001180305.1:n.2969-5C>T
NM_001193376.2:c.2969-5C>T	NP_001180305.1:n.2969-5C>T
NM_001193376.3:c.2969-5C>T	NP_001180305.1:n.2969-5C>T
NM_198253.2:c.3158-5C>T , LRG_343t1:c.3158-5C>T	NP_937983.2:n.3158-5C>T
NR_149162.1:n.2845-5C>T
NR_149162.2:n.2866-5C>T
NR_149162.3:n.2866-5C>T
NR_149163.1:n.2809-5C>T
NR_149163.2:n.2830-5C>T
NR_149163.3:n.2830-5C>T
ENST00000310581.9:c.3158-5C>T	ENSP00000309572.5:n.3158-5C>T
ENST00000334602.10:c.2969-5C>T	ENSP00000334346.6:n.2969-5C>T
ENST00000460137.6:c.2751-5C>T	ENSP00000425003.1:n.2751-5C>T
ENST00000484238.6:n.1600-5C>T
ENST00000656021.1:c.*2704-5C>T	ENSP00000499759.1:n.*2704-5C>T
XM_011514104.1:c.1628-5C>T	XP_011512406.1:n.1628-5C>T
XM_011514105.1:c.1514-5C>T	XP_011512407.1:n.1514-5C>T
XM_011514106.1:c.1514-5C>T	XP_011512408.1:n.1514-5C>T
XR_925683.1:n.287-164G>A