Canonical Allele Identifier: CA1180535183

Gene: TGFBR3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.91866969C= , CM000663.2:g.91866969C=	GRCh38
NC_000001.10:g.92332526C= , CM000663.1:g.92332526C=	GRCh37
NC_000001.9:g.92105114C=	NCBI36
NG_027757.1:g.44034G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000212355.9:c.-113-5325G= MANE Select	ENSP00000212355.4:n.-113-5325G=
ENST00000212355.8:c.-113-5325G=	ENSP00000212355.4:n.-113-5325G=
ENST00000370399.6:c.-113-5325G=	ENSP00000359426.2:n.-113-5325G=
ENST00000417833.2:c.-200-127G=	ENSP00000395975.2:n.-200-127G=
ENST00000465892.6:c.-113-5325G=	ENSP00000432638.1:n.-113-5325G=
ENST00000532540.5:c.-113-5325G=	ENSP00000434994.1:n.-113-5325G=
ENST00000533370.1:n.123-2690G=
NM_001195683.1:c.-113-5325G=	NP_001182612.1:n.-113-5325G=
NM_001195684.1:c.-113-5325G=	NP_001182613.1:n.-113-5325G=
NM_003243.4:c.-113-5325G=	NP_003234.2:n.-113-5325G=
NR_036634.1:n.403-5325G=
XM_006710867.1:c.-113-5325G=	XP_006710930.1:n.-113-5325G=
XM_006710867.2:c.-113-5325G=	XP_006710930.1:n.-113-5325G=
NM_003243.5:c.-113-5325G= MANE Select	NP_003234.2:n.-113-5325G=
NM_001195683.2:c.-113-5325G=	NP_001182612.1:n.-113-5325G=
NR_036634.2:n.275-5325G=