Canonical Allele Identifier: CA2690966464

Gene: TGFBR1

Linked Data

• gnomAD v4: 9-99146356-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146358_99146359del , CM000671.2:g.99146358_99146359del	GRCh38
NC_000009.11:g.101908640_101908641del , CM000671.1:g.101908640_101908641del	GRCh37
NC_000009.10:g.100948461_100948462del	NCBI36
NG_007461.1:g.46229_46230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.924-127_924-126del	ENSP00000449934.2:n.924-127_924-126del
ENST00000552573.7:c.936-127_936-126del	ENSP00000447182.3:n.936-127_936-126del
ENST00000548365.6:c.*53-127_*53-126del	ENSP00000448518.2:n.*53-127_*53-126del
ENST00000549021.6:c.693-127_693-126del	ENSP00000449028.2:n.693-127_693-126del
ENST00000698941.1:c.936-127_936-126del	ENSP00000514048.1:n.936-127_936-126del
ENST00000698942.1:c.*927-127_*927-126del	ENSP00000514049.1:n.*927-127_*927-126del
ENST00000374994.9:c.1131-127_1131-126del MANE Select	ENSP00000364133.4:n.1131-127_1131-126del
ENST00000374990.6:c.900-127_900-126del	ENSP00000364129.2:n.900-127_900-126del
ENST00000374994.8:c.1131-127_1131-126del	ENSP00000364133.4:n.1131-127_1131-126del
ENST00000549766.5:c.1143-1296_1143-1295del	ENSP00000446685.1:n.1143-1296_1143-1295del
ENST00000550253.1:c.924-127_924-126del	ENSP00000450052.1:n.924-127_924-126del
ENST00000552516.5:c.1143-127_1143-126del	ENSP00000447297.1:n.1143-127_1143-126del
NM_001130916.1:c.900-127_900-126del	NP_001124388.1:n.900-127_900-126del
NM_001130916.2:c.900-127_900-126del	NP_001124388.1:n.900-127_900-126del
NM_001306210.1:c.1143-127_1143-126del	NP_001293139.1:n.1143-127_1143-126del
NM_004612.2:c.1131-127_1131-126del	NP_004603.1:n.1131-127_1131-126del
NM_004612.3:c.1131-127_1131-126del	NP_004603.1:n.1131-127_1131-126del
XM_011518948.1:c.936-127_936-126del	XP_011517250.1:n.936-127_936-126del
XM_011518949.1:c.924-127_924-126del	XP_011517251.1:n.924-127_924-126del
XM_011518950.1:c.693-127_693-126del	XP_011517252.1:n.693-127_693-126del
XM_011518948.2:c.936-127_936-126del	XP_011517250.1:n.936-127_936-126del
XM_011518949.2:c.924-127_924-126del	XP_011517251.1:n.924-127_924-126del
XM_011518950.2:c.693-127_693-126del	XP_011517252.1:n.693-127_693-126del
XM_017015063.1:c.936-127_936-126del	XP_016870552.1:n.936-127_936-126del
XM_024447658.1:c.924-127_924-126del	XP_024303426.1:n.924-127_924-126del
NM_004612.4:c.1131-127_1131-126del MANE Select	NP_004603.1:n.1131-127_1131-126del
NM_001130916.3:c.900-127_900-126del	NP_001124388.1:n.900-127_900-126del
NM_001306210.2:c.1143-127_1143-126del	NP_001293139.1:n.1143-127_1143-126del