Canonical Allele Identifier: CA374231375

Gene: TGFBR1

Linked Data

• dbSNP Id: rs2118804566
• MyVariant Identifiers: chr9:g.101907066G>C (hg19) ; chr9:g.99144784G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99144784G>C , CM000671.2:g.99144784G>C	GRCh38
NC_000009.11:g.101907066G>C , CM000671.1:g.101907066G>C	GRCh37
NC_000009.10:g.100946887G>C	NCBI36
NG_007461.1:g.44655G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.819G>C	ENSP00000449934.2:p.Lys273Asn
ENST00000552573.7:c.831G>C	ENSP00000447182.3:p.Lys277Asn
ENST00000548365.6:c.600G>C	ENSP00000448518.2:p.Lys200Asn
ENST00000549021.6:c.588G>C	ENSP00000449028.2:p.Lys196Asn
ENST00000698941.1:c.831G>C	ENSP00000514048.1:p.Lys277Asn
ENST00000698942.1:c.*822G>C	ENSP00000514049.1:n.*822G>C
ENST00000374994.9:c.1026G>C MANE Select	ENSP00000364133.4:p.Lys342Asn
ENST00000374990.6:c.795G>C	ENSP00000364129.2:p.Lys265Asn
ENST00000374994.8:c.1026G>C	ENSP00000364133.4:p.Lys342Asn
ENST00000549766.5:c.1038G>C	ENSP00000446685.1:p.Lys346Asn
ENST00000550253.1:c.819G>C	ENSP00000450052.1:p.Lys273Asn
ENST00000552516.5:c.1038G>C	ENSP00000447297.1:p.Lys346Asn
NM_001130916.1:c.795G>C	NP_001124388.1:p.Lys265Asn
NM_001130916.2:c.795G>C	NP_001124388.1:p.Lys265Asn
NM_001306210.1:c.1038G>C	NP_001293139.1:p.Lys346Asn
NM_004612.2:c.1026G>C	NP_004603.1:p.Lys342Asn
NM_004612.3:c.1026G>C	NP_004603.1:p.Lys342Asn
XM_011518948.1:c.831G>C	XP_011517250.1:p.Lys277Asn
XM_011518949.1:c.819G>C	XP_011517251.1:p.Lys273Asn
XM_011518950.1:c.588G>C	XP_011517252.1:p.Lys196Asn
XM_011518948.2:c.831G>C	XP_011517250.1:p.Lys277Asn
XM_011518949.2:c.819G>C	XP_011517251.1:p.Lys273Asn
XM_011518950.2:c.588G>C	XP_011517252.1:p.Lys196Asn
XM_017015063.1:c.831G>C	XP_016870552.1:p.Lys277Asn
XM_024447658.1:c.819G>C	XP_024303426.1:p.Lys273Asn
NM_004612.4:c.1026G>C MANE Select	NP_004603.1:p.Lys342Asn
NM_001130916.3:c.795G>C	NP_001124388.1:p.Lys265Asn
NM_001306210.2:c.1038G>C	NP_001293139.1:p.Lys346Asn