Canonical Allele Identifier: CA383714148
Gene: TPI1 HGNC NCBI

Linked Data

gnomAD v4: 12-6870356-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870356C>G , CM000674.2:g.6870356C>G GRCh38
NC_000012.11:g.6979520C>G , CM000674.1:g.6979520C>G GRCh37
NC_000012.10:g.6849781C>G NCBI36
NG_011948.1:g.7937C>G
NG_013308.1:g.8002G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396705.10:c.723C>G MANE Select ENSP00000379933.4:p.Phe241Leu
ENST00000229270.8:c.834C>G ENSP00000229270.4:p.Phe278Leu
ENST00000396705.9:c.723C>G ENSP00000379933.4:p.Phe241Leu
ENST00000474253.1:n.212C>G
ENST00000488464.6:c.477C>G ENSP00000475620.1:p.Phe159Leu
ENST00000535434.5:c.477C>G ENSP00000443599.1:p.Phe159Leu
ENST00000613953.4:c.834C>G ENSP00000484435.1:p.Phe278Leu
NM_000365.5:c.723C>G NP_000356.1:p.Phe241Leu
NM_001159287.1:c.834C>G NP_001152759.1:p.Phe278Leu
NM_001258026.1:c.477C>G NP_001244955.1:p.Phe159Leu
XR_002957378.1:n.1731C>G
NM_000365.6:c.723C>G MANE Select NP_000356.1:p.Phe241Leu
NM_001258026.2:c.477C>G NP_001244955.1:p.Phe159Leu