Canonical Allele Identifier: CA1867259783

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142297_99142300delinsAATG , CM000671.2:g.99142297_99142300delinsAATG	GRCh38
NC_000009.11:g.101904579_101904582delinsAATG , CM000671.1:g.101904579_101904582delinsAATG	GRCh37
NC_000009.10:g.100944400_100944403delinsAATG	NCBI36
NG_007461.1:g.42168_42171delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.599-239_599-236delinsAATG	ENSP00000449934.2:n.599-239_599-236delinsAATG
ENST00000552573.7:c.611-239_611-236delinsAATG	ENSP00000447182.3:n.611-239_611-236delinsAATG
ENST00000548365.6:c.380-239_380-236delinsAATG	ENSP00000448518.2:n.380-239_380-236delinsAATG
ENST00000549021.6:c.368-239_368-236delinsAATG	ENSP00000449028.2:n.368-239_368-236delinsAATG
ENST00000698941.1:c.611-239_611-236delinsAATG	ENSP00000514048.1:n.611-239_611-236delinsAATG
ENST00000698942.1:c.*602-239_*602-236delinsAATG	ENSP00000514049.1:n.*602-239_*602-236delinsAATG
ENST00000374994.9:c.806-239_806-236delinsAATG MANE Select	ENSP00000364133.4:n.806-239_806-236delinsAATG
ENST00000374990.6:c.575-239_575-236delinsAATG	ENSP00000364129.2:n.575-239_575-236delinsAATG
ENST00000374994.8:c.806-239_806-236delinsAATG	ENSP00000364133.4:n.806-239_806-236delinsAATG
ENST00000549766.5:c.818-239_818-236delinsAATG	ENSP00000446685.1:n.818-239_818-236delinsAATG
ENST00000550253.1:c.599-239_599-236delinsAATG	ENSP00000450052.1:n.599-239_599-236delinsAATG
ENST00000552516.5:c.818-239_818-236delinsAATG	ENSP00000447297.1:n.818-239_818-236delinsAATG
NM_001130916.1:c.575-239_575-236delinsAATG	NP_001124388.1:n.575-239_575-236delinsAATG
NM_001130916.2:c.575-239_575-236delinsAATG	NP_001124388.1:n.575-239_575-236delinsAATG
NM_001306210.1:c.818-239_818-236delinsAATG	NP_001293139.1:n.818-239_818-236delinsAATG
NM_004612.2:c.806-239_806-236delinsAATG	NP_004603.1:n.806-239_806-236delinsAATG
NM_004612.3:c.806-239_806-236delinsAATG	NP_004603.1:n.806-239_806-236delinsAATG
XM_011518948.1:c.611-239_611-236delinsAATG	XP_011517250.1:n.611-239_611-236delinsAATG
XM_011518949.1:c.599-239_599-236delinsAATG	XP_011517251.1:n.599-239_599-236delinsAATG
XM_011518950.1:c.368-239_368-236delinsAATG	XP_011517252.1:n.368-239_368-236delinsAATG
XM_011518948.2:c.611-239_611-236delinsAATG	XP_011517250.1:n.611-239_611-236delinsAATG
XM_011518949.2:c.599-239_599-236delinsAATG	XP_011517251.1:n.599-239_599-236delinsAATG
XM_011518950.2:c.368-239_368-236delinsAATG	XP_011517252.1:n.368-239_368-236delinsAATG
XM_017015063.1:c.611-239_611-236delinsAATG	XP_016870552.1:n.611-239_611-236delinsAATG
XM_024447658.1:c.599-239_599-236delinsAATG	XP_024303426.1:n.599-239_599-236delinsAATG
NM_004612.4:c.806-239_806-236delinsAATG MANE Select	NP_004603.1:n.806-239_806-236delinsAATG
NM_001130916.3:c.575-239_575-236delinsAATG	NP_001124388.1:n.575-239_575-236delinsAATG
NM_001306210.2:c.818-239_818-236delinsAATG	NP_001293139.1:n.818-239_818-236delinsAATG