Canonical Allele Identifier: CA368526097

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100225270G>A (hg19) ; chr7:g.100627647G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627647G>A , CM000669.2:g.100627647G>A	GRCh38
NC_000007.13:g.100225270G>A , CM000669.1:g.100225270G>A	GRCh37
NC_000007.12:g.100063206G>A	NCBI36
NG_007989.1:g.18904C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.1697C>T MANE Select	ENSP00000223051.3:p.Pro566Leu
ENST00000223051.7:c.1697C>T	ENSP00000223051.3:p.Pro566Leu
ENST00000431692.5:c.*372C>T	ENSP00000413905.1:n.*372C>T
ENST00000462090.5:n.648C>T
ENST00000462107.1:c.1697C>T	ENSP00000420525.1:p.Pro566Leu
ENST00000465294.5:n.1532C>T
ENST00000473374.5:n.770C>T
ENST00000473963.1:n.726C>T
ENST00000476304.5:n.1318C>T
ENST00000490084.5:c.1050C>T
NM_001206855.1:c.1184C>T	NP_001193784.1:p.Pro395Leu
NM_003227.3:c.1697C>T	NP_003218.2:p.Pro566Leu
XM_005250553.3:c.1697C>T	XP_005250610.1:p.Pro566Leu
XM_005250554.3:c.1697C>T	XP_005250611.1:p.Pro566Leu
XR_927814.1:n.434-3509G>A
NM_001206855.2:c.1184C>T	NP_001193784.1:p.Pro395Leu
XM_005250553.4:c.1697C>T	XP_005250610.1:p.Pro566Leu
XM_017012573.1:c.1697C>T	XP_016868062.1:p.Pro566Leu
NM_003227.4:c.1697C>T MANE Select	NP_003218.2:p.Pro566Leu
NM_001206855.3:c.1184C>T	NP_001193784.1:p.Pro395Leu