Canonical Allele Identifier: CA2014289822

Gene: TPI1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870642_6870645delinsCGTG , CM000674.2:g.6870642_6870645delinsCGTG	GRCh38
NC_000012.11:g.6979806_6979809delinsCGTG , CM000674.1:g.6979806_6979809delinsCGTG	GRCh37
NC_000012.10:g.6850067_6850070delinsCGTG	NCBI36
NG_011948.1:g.8223_8226delinsCGTG
NG_013308.1:g.7713_7716delinsCACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*259_*262delinsCGTG MANE Select	ENSP00000379933.4:n.*259_*262delinsCGTG
ENST00000229270.8:c.*259_*262delinsCGTG	ENSP00000229270.4:n.*259_*262delinsCGTG
ENST00000396705.9:c.*259_*262delinsCGTG	ENSP00000379933.4:n.*259_*262delinsCGTG
ENST00000535434.5:c.*259_*262delinsCGTG	ENSP00000443599.1:n.*259_*262delinsCGTG
ENST00000613953.4:c.*259_*262delinsCGTG	ENSP00000484435.1:n.*259_*262delinsCGTG
NM_000365.5:c.*259_*262delinsCGTG	NP_000356.1:n.*259_*262delinsCGTG
NM_001159287.1:c.*259_*262delinsCGTG	NP_001152759.1:n.*259_*262delinsCGTG
NM_001258026.1:c.*259_*262delinsCGTG	NP_001244955.1:n.*259_*262delinsCGTG
XR_002957378.1:n.2017_2020delinsCGTG
NM_000365.6:c.*259_*262delinsCGTG MANE Select	NP_000356.1:n.*259_*262delinsCGTG
NM_001258026.2:c.*259_*262delinsCGTG	NP_001244955.1:n.*259_*262delinsCGTG