Canonical Allele Identifier: CA14301094

Gene: TERF2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.69373083A>G , CM000678.2:g.69373083A>G	GRCh38
NC_000016.9:g.69406986A>G , CM000678.1:g.69406986A>G	GRCh37
NC_000016.8:g.67964487A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254942.8:c.607-728T>C MANE Select	ENSP00000254942.3:n.607-728T>C
ENST00000254942.7:c.607-728T>C	ENSP00000254942.3:n.607-728T>C
ENST00000566257.5:c.118-728T>C	ENSP00000457094.1:n.118-728T>C
ENST00000566750.5:c.244-728T>C	ENSP00000456022.1:n.244-728T>C
ENST00000567296.6:c.607-728T>C	ENSP00000454955.2:n.607-728T>C
ENST00000567841.1:c.172-728T>C	ENSP00000476905.1:n.172-728T>C
ENST00000569280.1:c.331-728T>C
ENST00000569542.6:c.72-4601T>C
ENST00000569611.6:n.235-728T>C
NM_005652.4:c.607-728T>C	NP_005643.2:n.607-728T>C
XM_005256121.2:c.607-728T>C	XP_005256178.1:n.607-728T>C
XM_005256122.2:c.607-728T>C	XP_005256179.1:n.607-728T>C
XM_005256123.2:c.607-728T>C	XP_005256180.1:n.607-728T>C
XM_005256124.2:c.607-4601T>C	XP_005256181.1:n.607-4601T>C
XM_011523308.1:c.607-728T>C	XP_011521610.1:n.607-728T>C
XM_005256121.3:c.607-728T>C	XP_005256178.1:n.607-728T>C
XM_005256122.3:c.607-728T>C	XP_005256179.1:n.607-728T>C
XM_005256123.3:c.607-728T>C	XP_005256180.1:n.607-728T>C
XM_005256124.4:c.607-4601T>C	XP_005256181.1:n.607-4601T>C
XR_001751974.1:n.640-728T>C
NM_005652.5:c.607-728T>C MANE Select	NP_005643.2:n.607-728T>C