Canonical Allele Identifier: CA2777155179

Gene: TFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627693G>A , CM000669.2:g.100627693G>A	GRCh38
NC_000007.13:g.100225316G>A , CM000669.1:g.100225316G>A	GRCh37
NC_000007.12:g.100063252G>A	NCBI36
NG_007989.1:g.18858C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.1683-32C>T MANE Select	ENSP00000223051.3:n.1683-32C>T
ENST00000223051.7:c.1683-32C>T	ENSP00000223051.3:n.1683-32C>T
ENST00000431692.5:c.*358-32C>T	ENSP00000413905.1:n.*358-32C>T
ENST00000462090.5:n.634-32C>T
ENST00000462107.1:c.1683-32C>T	ENSP00000420525.1:n.1683-32C>T
ENST00000465294.5:n.1518-32C>T
ENST00000473374.5:n.756-32C>T
ENST00000473963.1:n.712-32C>T
ENST00000476304.5:n.1304-32C>T
ENST00000490084.5:c.1036-32C>T
NM_001206855.1:c.1170-32C>T	NP_001193784.1:n.1170-32C>T
NM_003227.3:c.1683-32C>T	NP_003218.2:n.1683-32C>T
XM_005250553.3:c.1683-32C>T	XP_005250610.1:n.1683-32C>T
XM_005250554.3:c.1683-32C>T	XP_005250611.1:n.1683-32C>T
XR_927814.1:n.434-3463G>A
NM_001206855.2:c.1170-32C>T	NP_001193784.1:n.1170-32C>T
XM_005250553.4:c.1683-32C>T	XP_005250610.1:n.1683-32C>T
XM_017012573.1:c.1683-32C>T	XP_016868062.1:n.1683-32C>T
NM_003227.4:c.1683-32C>T MANE Select	NP_003218.2:n.1683-32C>T
NM_001206855.3:c.1170-32C>T	NP_001193784.1:n.1170-32C>T