Canonical Allele Identifier: CA2617355790

Gene: TPI1

Linked Data

• gnomAD v4: 12-6870554-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870554G>T , CM000674.2:g.6870554G>T	GRCh38
NC_000012.11:g.6979718G>T , CM000674.1:g.6979718G>T	GRCh37
NC_000012.10:g.6849979G>T	NCBI36
NG_011948.1:g.8135G>T
NG_013308.1:g.7804C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*171G>T MANE Select	ENSP00000379933.4:n.*171G>T
ENST00000229270.8:c.*171G>T	ENSP00000229270.4:n.*171G>T
ENST00000396705.9:c.*171G>T	ENSP00000379933.4:n.*171G>T
ENST00000474253.1:n.410G>T
ENST00000535434.5:c.*171G>T	ENSP00000443599.1:n.*171G>T
ENST00000613953.4:c.*171G>T	ENSP00000484435.1:n.*171G>T
NM_000365.5:c.*171G>T	NP_000356.1:n.*171G>T
NM_001159287.1:c.*171G>T	NP_001152759.1:n.*171G>T
NM_001258026.1:c.*171G>T	NP_001244955.1:n.*171G>T
XR_002957378.1:n.1929G>T
NM_000365.6:c.*171G>T MANE Select	NP_000356.1:n.*171G>T
NM_001258026.2:c.*171G>T	NP_001244955.1:n.*171G>T