Canonical Allele Identifier: CA1140465839
Gene: TGFBR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91745463G= , CM000663.2:g.91745463G= GRCh38
NC_000001.10:g.92211020G= , CM000663.1:g.92211020G= GRCh37
NC_000001.9:g.91983608G= NCBI36
NG_027757.1:g.165540C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000212355.9:c.385-10504C= MANE Select ENSP00000212355.4:n.385-10504C=
ENST00000212355.8:c.385-10504C= ENSP00000212355.4:n.385-10504C=
ENST00000370399.6:c.385-10504C= ENSP00000359426.2:n.385-10504C=
ENST00000465892.6:c.385-10504C= ENSP00000432638.1:n.385-10504C=
ENST00000468996.2:n.187-10504C=
ENST00000525962.5:c.385-10504C= ENSP00000436127.1:n.385-10504C=
ENST00000532540.5:c.*332-10504C= ENSP00000434994.1:n.*332-10504C=
ENST00000533089.5:c.*412+9532C= ENSP00000433477.1:n.*412+9532C=
NM_001195683.1:c.385-10504C= NP_001182612.1:n.385-10504C=
NM_001195684.1:c.385-10504C= NP_001182613.1:n.385-10504C=
NM_003243.4:c.385-10504C= NP_003234.2:n.385-10504C=
NR_036634.1:n.997-10504C=
XM_006710867.1:c.385-10504C= XP_006710930.1:n.385-10504C=
XM_006710868.1:c.385-10504C= XP_006710931.1:n.385-10504C=
XM_011542058.1:c.-282-10504C= XP_011540360.1:n.-282-10504C=
XM_006710867.2:c.385-10504C= XP_006710930.1:n.385-10504C=
NM_003243.5:c.385-10504C= MANE Select NP_003234.2:n.385-10504C=
NM_001195683.2:c.385-10504C= NP_001182612.1:n.385-10504C=
NR_036634.2:n.869-10504C=