Canonical Allele Identifier: CA390468822

Gene: TGFB3 IFT43

Linked Data

• ClinVar Variation Id: 1024643
• ClinVar RCV Id: RCV002546118
• dbSNP Id: rs2035211931
• MyVariant Identifiers: chr14:g.76431943T>C (hg19) ; chr14:g.75965600T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75965600T>C , CM000676.2:g.75965600T>C	GRCh38
NC_000014.8:g.76431943T>C , CM000676.1:g.76431943T>C	GRCh37
NC_000014.7:g.75501696T>C	NCBI36
NG_011715.1:g.21150A>G , LRG_399:g.21150A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000238682.8:c.742A>G (TGFB3) MANE Select	ENSP00000238682.3:p.Ile248Val
ENST00000556674.2:c.742A>G (TGFB3)	ENSP00000502685.1:p.Ile248Val
ENST00000238682.7:c.742A>G (TGFB3)	ENSP00000238682.3:p.Ile248Val
ENST00000554980.5:n.1123A>G (TGFB3)
ENST00000555677.5:n.90-23285T>C (IFT43)
ENST00000556285.1:c.742A>G (TGFB3)	ENSP00000451110.1:p.Ile248Val
ENST00000557493.1:n.208A>G (TGFB3)
NM_003239.3:c.742A>G (TGFB3)	NP_003230.1:p.Ile248Val
XM_005268028.1:c.742A>G (TGFB3)	XP_005268085.1:p.Ile248Val
NM_001329938.1:c.742A>G (TGFB3)	NP_001316867.1:p.Ile248Val
NM_001329939.1:c.742A>G (TGFB3)	NP_001316868.1:p.Ile248Val
NM_003239.4:c.742A>G (TGFB3)	NP_003230.1:p.Ile248Val
NM_001329938.2:c.742A>G (TGFB3)	NP_001316867.1:p.Ile248Val
NM_001329939.2:c.742A>G (TGFB3)	NP_001316868.1:p.Ile248Val
NM_003239.5:c.742A>G (TGFB3) MANE Select	NP_003230.1:p.Ile248Val