Canonical Allele Identifier: CA1867263580

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146336_99146337delinsTG , CM000671.2:g.99146336_99146337delinsTG	GRCh38
NC_000009.11:g.101908618_101908619delinsTG , CM000671.1:g.101908618_101908619delinsTG	GRCh37
NC_000009.10:g.100948439_100948440delinsTG	NCBI36
NG_007461.1:g.46207_46208delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.924-149_924-148delinsTG	ENSP00000449934.2:n.924-149_924-148delinsTG
ENST00000552573.7:c.936-149_936-148delinsTG	ENSP00000447182.3:n.936-149_936-148delinsTG
ENST00000548365.6:c.*53-149_*53-148delinsTG	ENSP00000448518.2:n.*53-149_*53-148delinsTG
ENST00000549021.6:c.693-149_693-148delinsTG	ENSP00000449028.2:n.693-149_693-148delinsTG
ENST00000698941.1:c.936-149_936-148delinsTG	ENSP00000514048.1:n.936-149_936-148delinsTG
ENST00000698942.1:c.*927-149_*927-148delinsTG	ENSP00000514049.1:n.*927-149_*927-148delinsTG
ENST00000374994.9:c.1131-149_1131-148delinsTG MANE Select	ENSP00000364133.4:n.1131-149_1131-148delinsTG
ENST00000374990.6:c.900-149_900-148delinsTG	ENSP00000364129.2:n.900-149_900-148delinsTG
ENST00000374994.8:c.1131-149_1131-148delinsTG	ENSP00000364133.4:n.1131-149_1131-148delinsTG
ENST00000549766.5:c.1143-1318_1143-1317delinsTG	ENSP00000446685.1:n.1143-1318_1143-1317delinsTG
ENST00000550253.1:c.924-149_924-148delinsTG	ENSP00000450052.1:n.924-149_924-148delinsTG
ENST00000552516.5:c.1143-149_1143-148delinsTG	ENSP00000447297.1:n.1143-149_1143-148delinsTG
NM_001130916.1:c.900-149_900-148delinsTG	NP_001124388.1:n.900-149_900-148delinsTG
NM_001130916.2:c.900-149_900-148delinsTG	NP_001124388.1:n.900-149_900-148delinsTG
NM_001306210.1:c.1143-149_1143-148delinsTG	NP_001293139.1:n.1143-149_1143-148delinsTG
NM_004612.2:c.1131-149_1131-148delinsTG	NP_004603.1:n.1131-149_1131-148delinsTG
NM_004612.3:c.1131-149_1131-148delinsTG	NP_004603.1:n.1131-149_1131-148delinsTG
XM_011518948.1:c.936-149_936-148delinsTG	XP_011517250.1:n.936-149_936-148delinsTG
XM_011518949.1:c.924-149_924-148delinsTG	XP_011517251.1:n.924-149_924-148delinsTG
XM_011518950.1:c.693-149_693-148delinsTG	XP_011517252.1:n.693-149_693-148delinsTG
XM_011518948.2:c.936-149_936-148delinsTG	XP_011517250.1:n.936-149_936-148delinsTG
XM_011518949.2:c.924-149_924-148delinsTG	XP_011517251.1:n.924-149_924-148delinsTG
XM_011518950.2:c.693-149_693-148delinsTG	XP_011517252.1:n.693-149_693-148delinsTG
XM_017015063.1:c.936-149_936-148delinsTG	XP_016870552.1:n.936-149_936-148delinsTG
XM_024447658.1:c.924-149_924-148delinsTG	XP_024303426.1:n.924-149_924-148delinsTG
NM_004612.4:c.1131-149_1131-148delinsTG MANE Select	NP_004603.1:n.1131-149_1131-148delinsTG
NM_001130916.3:c.900-149_900-148delinsTG	NP_001124388.1:n.900-149_900-148delinsTG
NM_001306210.2:c.1143-149_1143-148delinsTG	NP_001293139.1:n.1143-149_1143-148delinsTG