Canonical Allele Identifier: CA368533485

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100230624C>A (hg19) ; chr7:g.100633001C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633001C>A , CM000669.2:g.100633001C>A	GRCh38
NC_000007.13:g.100230624C>A , CM000669.1:g.100230624C>A	GRCh37
NC_000007.12:g.100068560C>A	NCBI36
NG_007989.1:g.13550G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.849G>T MANE Select	ENSP00000223051.3:p.Lys283Asn
ENST00000223051.7:c.849G>T	ENSP00000223051.3:p.Lys283Asn
ENST00000431692.5:c.849G>T	ENSP00000413905.1:p.Lys283Asn
ENST00000462090.5:n.90G>T
ENST00000462107.1:c.849G>T	ENSP00000420525.1:p.Lys283Asn
ENST00000465294.5:n.854G>T
ENST00000473374.5:n.299G>T
ENST00000473571.1:n.303G>T
ENST00000475011.1:n.378G>T
ENST00000476304.5:n.470G>T
ENST00000490084.5:c.104G>T
NM_001206855.1:c.336G>T	NP_001193784.1:p.Lys112Asn
NM_003227.3:c.849G>T	NP_003218.2:p.Lys283Asn
XM_005250553.3:c.849G>T	XP_005250610.1:p.Lys283Asn
XM_005250554.3:c.849G>T	XP_005250611.1:p.Lys283Asn
XR_927814.1:n.582C>A
NM_001206855.2:c.336G>T	NP_001193784.1:p.Lys112Asn
XM_005250553.4:c.849G>T	XP_005250610.1:p.Lys283Asn
XM_017012573.1:c.849G>T	XP_016868062.1:p.Lys283Asn
NM_003227.4:c.849G>T MANE Select	NP_003218.2:p.Lys283Asn
NM_001206855.3:c.336G>T	NP_001193784.1:p.Lys112Asn