Canonical Allele Identifier: CA112948829

Gene: TERT

Linked Data

• dbSNP Id: rs373644368
• gnomAD v2: 5-1278672-G-A
• gnomAD v3: 5-1278557-G-A
• gnomAD v4: 5-1278557-G-A
• MyVariant Identifiers: chr5:g.1278672G>A (hg19) ; chr5:g.1278557G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1278557G>A , CM000667.2:g.1278557G>A	GRCh38
NC_000005.9:g.1278672G>A , CM000667.1:g.1278672G>A	GRCh37
NC_000005.8:g.1331672G>A	NCBI36
NG_009265.1:g.21491C>T , LRG_343:g.21491C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310581.10:c.2286+84C>T MANE Select	ENSP00000309572.5:n.2286+84C>T
ENST00000656021.1:c.*1832+84C>T	ENSP00000499759.1:n.*1832+84C>T
ENST00000310581.9:c.2286+84C>T	ENSP00000309572.5:n.2286+84C>T
ENST00000334602.10:c.2286+84C>T	ENSP00000334346.6:n.2286+84C>T
ENST00000460137.6:c.2250+84C>T	ENSP00000425003.1:n.2250+84C>T
ENST00000484238.6:n.1099+84C>T
ENST00000508104.2:c.2286+84C>T	ENSP00000426042.2:n.2286+84C>T
NM_001193376.1:c.2286+84C>T	NP_001180305.1:n.2286+84C>T
NM_198253.2:c.2286+84C>T , LRG_343t1:c.2286+84C>T	NP_937983.2:n.2286+84C>T
XM_011514104.1:c.756+84C>T	XP_011512406.1:n.756+84C>T
XM_011514105.1:c.642+84C>T	XP_011512407.1:n.642+84C>T
XM_011514106.1:c.642+84C>T	XP_011512408.1:n.642+84C>T
NR_149162.1:n.2344+84C>T
NR_149163.1:n.2308+84C>T
NM_001193376.2:c.2286+84C>T	NP_001180305.1:n.2286+84C>T
NM_198253.3:c.2286+84C>T MANE Select	NP_937983.2:n.2286+84C>T
NR_149162.2:n.2365+84C>T
NR_149163.2:n.2329+84C>T
NM_001193376.3:c.2286+84C>T	NP_001180305.1:n.2286+84C>T
NR_149162.3:n.2365+84C>T
NR_149163.3:n.2329+84C>T