Canonical Allele Identifier: CA2014289598
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870218_6870234delinsAGACTCATCCCATTCTT , CM000674.2:g.6870218_6870234delinsAGACTCATCCCATTCTT GRCh38
NC_000012.11:g.6979382_6979398delinsAGACTCATCCCATTCTT , CM000674.1:g.6979382_6979398delinsAGACTCATCCCATTCTT GRCh37
NC_000012.10:g.6849643_6849659delinsAGACTCATCCCATTCTT NCBI36
NG_011948.1:g.7799_7815delinsAGACTCATCCCATTCTT
NG_013308.1:g.8124_8140delinsAAGAATGGGATGAGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.632-47_632-31delinsAGACTCATCCCATTCTT MANE Select ENSP00000379933.4:n.632-47_632-31delinsAGACTCATCCCATTCTT
ENST00000229270.8:c.743-47_743-31delinsAGACTCATCCCATTCTT ENSP00000229270.4:n.743-47_743-31delinsAGACTCATCCCATTCTT
ENST00000396705.9:c.632-47_632-31delinsAGACTCATCCCATTCTT ENSP00000379933.4:n.632-47_632-31delinsAGACTCATCCCATTCTT
ENST00000474253.1:n.121-47_121-31delinsAGACTCATCCCATTCTT
ENST00000488464.6:c.386-47_386-31delinsAGACTCATCCCATTCTT ENSP00000475620.1:n.386-47_386-31delinsAGACTCATCCCATTCTT
ENST00000535434.5:c.386-47_386-31delinsAGACTCATCCCATTCTT ENSP00000443599.1:n.386-47_386-31delinsAGACTCATCCCATTCTT
ENST00000613953.4:c.743-47_743-31delinsAGACTCATCCCATTCTT ENSP00000484435.1:n.743-47_743-31delinsAGACTCATCCCATTCTT
NM_000365.5:c.632-47_632-31delinsAGACTCATCCCATTCTT NP_000356.1:n.632-47_632-31delinsAGACTCATCCCATTCTT
NM_001159287.1:c.743-47_743-31delinsAGACTCATCCCATTCTT NP_001152759.1:n.743-47_743-31delinsAGACTCATCCCATTCTT
NM_001258026.1:c.386-47_386-31delinsAGACTCATCCCATTCTT NP_001244955.1:n.386-47_386-31delinsAGACTCATCCCATTCTT
XR_002957378.1:n.1640-47_1640-31delinsAGACTCATCCCATTCTT
NM_000365.6:c.632-47_632-31delinsAGACTCATCCCATTCTT MANE Select NP_000356.1:n.632-47_632-31delinsAGACTCATCCCATTCTT
NM_001258026.2:c.386-47_386-31delinsAGACTCATCCCATTCTT NP_001244955.1:n.386-47_386-31delinsAGACTCATCCCATTCTT