Canonical Allele Identifier: CA8279521

Gene: TSR1 SRR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2323275G>A , CM000679.2:g.2323275G>A	GRCh38
NC_000017.10:g.2226569G>A , CM000679.1:g.2226569G>A	GRCh37
NC_000017.9:g.2173319G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018128.5:c.*921C>T (TSR1) MANE Select	NP_060598.3:n.*921C>T
NM_021947.3:c.734G>A (SRR) MANE Select	NP_068766.1:p.Gly245Asp
ENST00000301364.10:c.*921C>T (TSR1) MANE Select	ENSP00000301364.4:n.*921C>T
ENST00000344595.10:c.734G>A (SRR) MANE Select	ENSP00000339435.5:p.Gly245Asp
NM_001304803.1:c.287G>A (SRR)	NP_001291732.1:p.Gly96Asp
NM_018128.4:c.*921C>T (TSR1)	NP_060598.3:n.*921C>T
NM_021947.2:c.734G>A (SRR)	NP_068766.1:p.Gly245Asp
ENST00000301364.9:c.*921C>T (TSR1)	ENSP00000301364.4:n.*921C>T
ENST00000344595.9:c.734G>A (SRR)	ENSP00000339435.5:p.Gly245Asp
ENST00000576848.1:c.56G>A (SRR)	ENSP00000476682.1:p.Gly19Asp
XM_006721565.2:c.734G>A (SRR)	XP_006721628.1:p.Gly245Asp
XM_006721565.3:c.734G>A (SRR)	XP_006721628.1:p.Gly245Asp
XM_006721566.2:c.734G>A (SRR)	XP_006721629.1:p.Gly245Asp
XM_006721566.3:c.734G>A (SRR)	XP_006721629.1:p.Gly245Asp
XM_011523974.1:c.734G>A (SRR)	XP_011522276.1:p.Gly245Asp
XM_011523974.3:c.734G>A (SRR)	XP_011522276.1:p.Gly245Asp
XM_011523975.1:c.734G>A (SRR)	XP_011522277.1:p.Gly245Asp