Canonical Allele Identifier: CA368534717

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100231064A>C (hg19) ; chr7:g.100633441A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633441A>C , CM000669.2:g.100633441A>C	GRCh38
NC_000007.13:g.100231064A>C , CM000669.1:g.100231064A>C	GRCh37
NC_000007.12:g.100069000A>C	NCBI36
NG_007989.1:g.13110T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.589T>G MANE Select	ENSP00000223051.3:p.Tyr197Asp
ENST00000223051.7:c.589T>G	ENSP00000223051.3:p.Tyr197Asp
ENST00000431692.5:c.589T>G	ENSP00000413905.1:p.Tyr197Asp
ENST00000462107.1:c.589T>G	ENSP00000420525.1:p.Tyr197Asp
ENST00000465294.5:n.594T>G
ENST00000475011.1:n.118T>G
ENST00000476304.5:n.210T>G
NM_001206855.1:c.76T>G	NP_001193784.1:p.Tyr26Asp
NM_003227.3:c.589T>G	NP_003218.2:p.Tyr197Asp
XM_005250553.3:c.589T>G	XP_005250610.1:p.Tyr197Asp
XM_005250554.3:c.589T>G	XP_005250611.1:p.Tyr197Asp
NM_001206855.2:c.76T>G	NP_001193784.1:p.Tyr26Asp
XM_005250553.4:c.589T>G	XP_005250610.1:p.Tyr197Asp
XM_017012573.1:c.589T>G	XP_016868062.1:p.Tyr197Asp
NM_003227.4:c.589T>G MANE Select	NP_003218.2:p.Tyr197Asp
NM_001206855.3:c.76T>G	NP_001193784.1:p.Tyr26Asp