Canonical Allele Identifier: CA368534132

Gene: TFR2

Linked Data

• gnomAD v4: 7-100633113-A-G
• MyVariant Identifiers: chr7:g.100230736A>G (hg19) ; chr7:g.100633113A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633113A>G , CM000669.2:g.100633113A>G	GRCh38
NC_000007.13:g.100230736A>G , CM000669.1:g.100230736A>G	GRCh37
NC_000007.12:g.100068672A>G	NCBI36
NG_007989.1:g.13438T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.737T>C MANE Select	ENSP00000223051.3:p.Val246Ala
ENST00000223051.7:c.737T>C	ENSP00000223051.3:p.Val246Ala
ENST00000431692.5:c.737T>C	ENSP00000413905.1:p.Val246Ala
ENST00000462107.1:c.737T>C	ENSP00000420525.1:p.Val246Ala
ENST00000465294.5:n.742T>C
ENST00000473374.5:n.187T>C
ENST00000473571.1:n.191T>C
ENST00000475011.1:n.266T>C
ENST00000476304.5:n.358T>C
NM_001206855.1:c.224T>C	NP_001193784.1:p.Val75Ala
NM_003227.3:c.737T>C	NP_003218.2:p.Val246Ala
XM_005250553.3:c.737T>C	XP_005250610.1:p.Val246Ala
XM_005250554.3:c.737T>C	XP_005250611.1:p.Val246Ala
NM_001206855.2:c.224T>C	NP_001193784.1:p.Val75Ala
XM_005250553.4:c.737T>C	XP_005250610.1:p.Val246Ala
XM_017012573.1:c.737T>C	XP_016868062.1:p.Val246Ala
NM_003227.4:c.737T>C MANE Select	NP_003218.2:p.Val246Ala
NM_001206855.3:c.224T>C	NP_001193784.1:p.Val75Ala