Canonical Allele Identifier: CA2014289648

Gene: TPI1

Linked Data

• dbSNP Id: rs1944559736
• gnomAD v4: 12-6870337-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870339del , CM000674.2:g.6870339del	GRCh38
NC_000012.11:g.6979503del , CM000674.1:g.6979503del	GRCh37
NC_000012.10:g.6849764del	NCBI36
NG_011948.1:g.7920del
NG_013308.1:g.8020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.706del MANE Select	ENSP00000379933.4:p.Ser236ProfsTer?
ENST00000229270.8:c.817del	ENSP00000229270.4:p.Ser273ProfsTer?
ENST00000396705.9:c.706del	ENSP00000379933.4:p.Ser236ProfsTer?
ENST00000474253.1:n.195del
ENST00000488464.6:c.460del	ENSP00000475620.1:p.Ser154ProfsTer?
ENST00000535434.5:c.460del	ENSP00000443599.1:p.Ser154ProfsTer?
ENST00000613953.4:c.817del	ENSP00000484435.1:p.Ser273ProfsTer?
NM_000365.5:c.706del	NP_000356.1:p.Ser236ProfsTer?
NM_001159287.1:c.817del	NP_001152759.1:p.Ser273ProfsTer?
NM_001258026.1:c.460del	NP_001244955.1:p.Ser154ProfsTer?
XR_002957378.1:n.1714del
NM_000365.6:c.706del MANE Select	NP_000356.1:p.Ser236ProfsTer?
NM_001258026.2:c.460del	NP_001244955.1:p.Ser154ProfsTer?