Canonical Allele Identifier: CA645570878

Gene: TPI1

Linked Data

• COSMIC: COSM6073333 ; COSM6073334

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870339_6870340delinsAA , CM000674.2:g.6870339_6870340delinsAA	GRCh38
NC_000012.11:g.6979503_6979504delinsAA , CM000674.1:g.6979503_6979504delinsAA	GRCh37
NC_000012.10:g.6849764_6849765delinsAA	NCBI36
NG_011948.1:g.7920_7921delinsAA
NG_013308.1:g.8018_8019delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.706_707delinsAA MANE Select	ENSP00000379933.4:p.Ser236Asn
ENST00000229270.8:c.817_818delinsAA	ENSP00000229270.4:p.Ser273Asn
ENST00000396705.9:c.706_707delinsAA	ENSP00000379933.4:p.Ser236Asn
ENST00000474253.1:n.195_196delinsAA
ENST00000488464.6:c.460_461delinsAA	ENSP00000475620.1:p.Ser154Asn
ENST00000535434.5:c.460_461delinsAA	ENSP00000443599.1:p.Ser154Asn
ENST00000613953.4:c.817_818delinsAA	ENSP00000484435.1:p.Ser273Asn
NM_000365.5:c.706_707delinsAA	NP_000356.1:p.Ser236Asn
NM_001159287.1:c.817_818delinsAA	NP_001152759.1:p.Ser273Asn
NM_001258026.1:c.460_461delinsAA	NP_001244955.1:p.Ser154Asn
XR_002957378.1:n.1714_1715delinsAA
NM_000365.6:c.706_707delinsAA MANE Select	NP_000356.1:p.Ser236Asn
NM_001258026.2:c.460_461delinsAA	NP_001244955.1:p.Ser154Asn