Canonical Allele Identifier: CA1354848159

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30617027_30617029delinsATG , CM000665.2:g.30617027_30617029delinsATG	GRCh38
NC_000003.11:g.30658519_30658521delinsATG , CM000665.1:g.30658519_30658521delinsATG	GRCh37
NC_000003.10:g.30633523_30633525delinsATG	NCBI36
NG_007490.1:g.15526_15528delinsATG , LRG_779:g.15526_15528delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+10050_94+10052delinsATG MANE Select	ENSP00000295754.5:n.94+10050_94+10052delinsATG
ENST00000673250.1:n.143+2321_143+2323delinsATG
ENST00000295754.9:c.94+10050_94+10052delinsATG	ENSP00000295754.5:n.94+10050_94+10052delinsATG
ENST00000359013.4:c.95-6172_95-6170delinsATG	ENSP00000351905.4:n.95-6172_95-6170delinsATG
NM_001024847.2:c.95-6172_95-6170delinsATG , LRG_779t1:c.95-6172_95-6170delinsATG	NP_001020018.1:n.95-6172_95-6170delinsATG
NM_003242.5:c.94+10050_94+10052delinsATG	NP_003233.4:n.94+10050_94+10052delinsATG
XM_011534043.1:c.46+2321_46+2323delinsATG	XP_011532345.1:n.46+2321_46+2323delinsATG
XM_011534044.1:c.46+2321_46+2323delinsATG	XP_011532346.1:n.46+2321_46+2323delinsATG
XM_011534045.1:c.-12+10434_-12+10436delinsATG	XP_011532347.1:n.-12+10434_-12+10436delinsATG
XM_011534043.2:c.46+2321_46+2323delinsATG	XP_011532345.1:n.46+2321_46+2323delinsATG
XM_011534045.3:c.-12+10434_-12+10436delinsATG	XP_011532347.1:n.-12+10434_-12+10436delinsATG
NM_003242.6:c.94+10050_94+10052delinsATG MANE Select	NP_003233.4:n.94+10050_94+10052delinsATG