Canonical Allele Identifier: CA456894292

Gene: TFR2

Linked Data

• gnomAD v4: 7-100627306-G-C
• MyVariant Identifiers: chr7:g.100224929G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627306G>C , CM000669.2:g.100627306G>C	GRCh38
NC_000007.13:g.100224929G>C , CM000669.1:g.100224929G>C	GRCh37
NC_000007.12:g.100062865G>C	NCBI36
NG_007989.1:g.19245C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.1953C>G MANE Select	ENSP00000223051.3:p.Leu651=
ENST00000223051.7:c.1953C>G	ENSP00000223051.3:p.Leu651=
ENST00000431692.5:c.*628C>G	ENSP00000413905.1:n.*628C>G
ENST00000461176.1:n.299C>G
ENST00000462090.5:n.989C>G
ENST00000462107.1:c.1953C>G	ENSP00000420525.1:p.Leu651=
ENST00000465294.5:n.1873C>G
ENST00000476304.5:n.1574C>G
ENST00000490084.5:c.1306C>G
NM_001206855.1:c.1440C>G	NP_001193784.1:p.Leu480=
NM_003227.3:c.1953C>G	NP_003218.2:p.Leu651=
XM_005250553.3:c.1953C>G	XP_005250610.1:p.Leu651=
XM_005250554.3:c.1953C>G	XP_005250611.1:p.Leu651=
XR_927814.1:n.434-3850G>C
NM_001206855.2:c.1440C>G	NP_001193784.1:p.Leu480=
XM_005250553.4:c.1953C>G	XP_005250610.1:p.Leu651=
XM_017012573.1:c.1953C>G	XP_016868062.1:p.Leu651=
NM_003227.4:c.1953C>G MANE Select	NP_003218.2:p.Leu651=
NM_001206855.3:c.1440C>G	NP_001193784.1:p.Leu480=