Canonical Allele Identifier: CA2522688065

Gene: TGFBR3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91705257_91705258insAC , CM000663.2:g.91705257_91705258insAC	GRCh38
NC_000001.10:g.92170814_92170815insAC , CM000663.1:g.92170814_92170815insAC	GRCh37
NC_000001.9:g.91943402_91943403insAC	NCBI36
NG_027757.1:g.205746_205747insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000212355.9:c.2287+3406_2287+3407insTG MANE Select	ENSP00000212355.4:n.2287+3406_2287+3407insTG
ENST00000212355.8:c.2287+3406_2287+3407insTG	ENSP00000212355.4:n.2287+3406_2287+3407insTG
ENST00000370399.6:c.2284+3406_2284+3407insTG	ENSP00000359426.2:n.2284+3406_2284+3407insTG
ENST00000465892.6:c.2284+3406_2284+3407insTG	ENSP00000432638.1:n.2284+3406_2284+3407insTG
ENST00000470600.1:n.242+3406_242+3407insTG
ENST00000525962.5:c.2287+3406_2287+3407insTG	ENSP00000436127.1:n.2287+3406_2287+3407insTG
ENST00000532540.5:c.*2234+3406_*2234+3407insTG	ENSP00000434994.1:n.*2234+3406_*2234+3407insTG
ENST00000533089.5:c.*2005+3406_*2005+3407insTG	ENSP00000433477.1:n.*2005+3406_*2005+3407insTG
NM_001195683.1:c.2284+3406_2284+3407insTG	NP_001182612.1:n.2284+3406_2284+3407insTG
NM_001195684.1:c.2284+3406_2284+3407insTG	NP_001182613.1:n.2284+3406_2284+3407insTG
NM_003243.4:c.2287+3406_2287+3407insTG	NP_003234.2:n.2287+3406_2287+3407insTG
NR_036634.1:n.2899+3406_2899+3407insTG
XM_006710867.1:c.2287+3406_2287+3407insTG	XP_006710930.1:n.2287+3406_2287+3407insTG
XM_006710868.1:c.2287+3406_2287+3407insTG	XP_006710931.1:n.2287+3406_2287+3407insTG
XM_011542058.1:c.1621+3406_1621+3407insTG	XP_011540360.1:n.1621+3406_1621+3407insTG
XM_006710867.2:c.2287+3406_2287+3407insTG	XP_006710930.1:n.2287+3406_2287+3407insTG
NM_003243.5:c.2287+3406_2287+3407insTG MANE Select	NP_003234.2:n.2287+3406_2287+3407insTG
NM_001195683.2:c.2284+3406_2284+3407insTG	NP_001182612.1:n.2284+3406_2284+3407insTG
NR_036634.2:n.2771+3406_2771+3407insTG