Canonical Allele Identifier: CA368525503

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100225098G>C (hg19) ; chr7:g.100627475G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627475G>C , CM000669.2:g.100627475G>C	GRCh38
NC_000007.13:g.100225098G>C , CM000669.1:g.100225098G>C	GRCh37
NC_000007.12:g.100063034G>C	NCBI36
NG_007989.1:g.19076C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.1784C>G MANE Select	ENSP00000223051.3:p.Pro595Arg
ENST00000223051.7:c.1784C>G	ENSP00000223051.3:p.Pro595Arg
ENST00000431692.5:c.*459C>G	ENSP00000413905.1:n.*459C>G
ENST00000461176.1:n.130C>G
ENST00000462090.5:n.820C>G
ENST00000462107.1:c.1784C>G	ENSP00000420525.1:p.Pro595Arg
ENST00000465294.5:n.1704C>G
ENST00000473374.5:n.857C>G
ENST00000476304.5:n.1405C>G
ENST00000490084.5:c.1137C>G
NM_001206855.1:c.1271C>G	NP_001193784.1:p.Pro424Arg
NM_003227.3:c.1784C>G	NP_003218.2:p.Pro595Arg
XM_005250553.3:c.1784C>G	XP_005250610.1:p.Pro595Arg
XM_005250554.3:c.1784C>G	XP_005250611.1:p.Pro595Arg
XR_927814.1:n.434-3681G>C
NM_001206855.2:c.1271C>G	NP_001193784.1:p.Pro424Arg
XM_005250553.4:c.1784C>G	XP_005250610.1:p.Pro595Arg
XM_017012573.1:c.1784C>G	XP_016868062.1:p.Pro595Arg
NM_003227.4:c.1784C>G MANE Select	NP_003218.2:p.Pro595Arg
NM_001206855.3:c.1271C>G	NP_001193784.1:p.Pro424Arg