Canonical Allele Identifier: CA368525150

Gene: TFR2

Linked Data

• gnomAD v4: 7-100627419-G-T
• MyVariant Identifiers: chr7:g.100225042G>T (hg19) ; chr7:g.100627419G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627419G>T , CM000669.2:g.100627419G>T	GRCh38
NC_000007.13:g.100225042G>T , CM000669.1:g.100225042G>T	GRCh37
NC_000007.12:g.100062978G>T	NCBI36
NG_007989.1:g.19132C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.1840C>A MANE Select	ENSP00000223051.3:p.Arg614Ser
ENST00000223051.7:c.1840C>A	ENSP00000223051.3:p.Arg614Ser
ENST00000431692.5:c.*515C>A	ENSP00000413905.1:n.*515C>A
ENST00000461176.1:n.186C>A
ENST00000462090.5:n.876C>A
ENST00000462107.1:c.1840C>A	ENSP00000420525.1:p.Arg614Ser
ENST00000465294.5:n.1760C>A
ENST00000476304.5:n.1461C>A
ENST00000490084.5:c.1193C>A
NM_001206855.1:c.1327C>A	NP_001193784.1:p.Arg443Ser
NM_003227.3:c.1840C>A	NP_003218.2:p.Arg614Ser
XM_005250553.3:c.1840C>A	XP_005250610.1:p.Arg614Ser
XM_005250554.3:c.1840C>A	XP_005250611.1:p.Arg614Ser
XR_927814.1:n.434-3737G>T
NM_001206855.2:c.1327C>A	NP_001193784.1:p.Arg443Ser
XM_005250553.4:c.1840C>A	XP_005250610.1:p.Arg614Ser
XM_017012573.1:c.1840C>A	XP_016868062.1:p.Arg614Ser
NM_003227.4:c.1840C>A MANE Select	NP_003218.2:p.Arg614Ser
NM_001206855.3:c.1327C>A	NP_001193784.1:p.Arg443Ser