Canonical Allele Identifier: CA2785270298

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142920_99142921insCG , CM000671.2:g.99142920_99142921insCG	GRCh38
NC_000009.11:g.101905202_101905203insCG , CM000671.1:g.101905202_101905203insCG	GRCh37
NC_000009.10:g.100945023_100945024insCG	NCBI36
NG_007461.1:g.42791_42792insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.766+217_766+218insCG	ENSP00000449934.2:n.766+217_766+218insCG
ENST00000552573.7:c.778+217_778+218insCG	ENSP00000447182.3:n.778+217_778+218insCG
ENST00000548365.6:c.547+217_547+218insCG	ENSP00000448518.2:n.547+217_547+218insCG
ENST00000549021.6:c.535+217_535+218insCG	ENSP00000449028.2:n.535+217_535+218insCG
ENST00000698941.1:c.778+217_778+218insCG	ENSP00000514048.1:n.778+217_778+218insCG
ENST00000698942.1:c.*769+217_*769+218insCG	ENSP00000514049.1:n.*769+217_*769+218insCG
ENST00000374994.9:c.973+217_973+218insCG MANE Select	ENSP00000364133.4:n.973+217_973+218insCG
ENST00000374990.6:c.742+217_742+218insCG	ENSP00000364129.2:n.742+217_742+218insCG
ENST00000374994.8:c.973+217_973+218insCG	ENSP00000364133.4:n.973+217_973+218insCG
ENST00000549766.5:c.985+217_985+218insCG	ENSP00000446685.1:n.985+217_985+218insCG
ENST00000550253.1:c.766+217_766+218insCG	ENSP00000450052.1:n.766+217_766+218insCG
ENST00000552516.5:c.985+217_985+218insCG	ENSP00000447297.1:n.985+217_985+218insCG
NM_001130916.1:c.742+217_742+218insCG	NP_001124388.1:n.742+217_742+218insCG
NM_001130916.2:c.742+217_742+218insCG	NP_001124388.1:n.742+217_742+218insCG
NM_001306210.1:c.985+217_985+218insCG	NP_001293139.1:n.985+217_985+218insCG
NM_004612.2:c.973+217_973+218insCG	NP_004603.1:n.973+217_973+218insCG
NM_004612.3:c.973+217_973+218insCG	NP_004603.1:n.973+217_973+218insCG
XM_011518948.1:c.778+217_778+218insCG	XP_011517250.1:n.778+217_778+218insCG
XM_011518949.1:c.766+217_766+218insCG	XP_011517251.1:n.766+217_766+218insCG
XM_011518950.1:c.535+217_535+218insCG	XP_011517252.1:n.535+217_535+218insCG
XM_011518948.2:c.778+217_778+218insCG	XP_011517250.1:n.778+217_778+218insCG
XM_011518949.2:c.766+217_766+218insCG	XP_011517251.1:n.766+217_766+218insCG
XM_011518950.2:c.535+217_535+218insCG	XP_011517252.1:n.535+217_535+218insCG
XM_017015063.1:c.778+217_778+218insCG	XP_016870552.1:n.778+217_778+218insCG
XM_024447658.1:c.766+217_766+218insCG	XP_024303426.1:n.766+217_766+218insCG
NM_004612.4:c.973+217_973+218insCG MANE Select	NP_004603.1:n.973+217_973+218insCG
NM_001130916.3:c.742+217_742+218insCG	NP_001124388.1:n.742+217_742+218insCG
NM_001306210.2:c.985+217_985+218insCG	NP_001293139.1:n.985+217_985+218insCG