Canonical Allele Identifier: CA2617355904

Gene: TPI1

Linked Data

• gnomAD v4: 12-6870604-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870604T>C , CM000674.2:g.6870604T>C	GRCh38
NC_000012.11:g.6979768T>C , CM000674.1:g.6979768T>C	GRCh37
NC_000012.10:g.6850029T>C	NCBI36
NG_011948.1:g.8185T>C
NG_013308.1:g.7754A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*221T>C MANE Select	ENSP00000379933.4:n.*221T>C
ENST00000229270.8:c.*221T>C	ENSP00000229270.4:n.*221T>C
ENST00000396705.9:c.*221T>C	ENSP00000379933.4:n.*221T>C
ENST00000535434.5:c.*221T>C	ENSP00000443599.1:n.*221T>C
ENST00000613953.4:c.*221T>C	ENSP00000484435.1:n.*221T>C
NM_000365.5:c.*221T>C	NP_000356.1:n.*221T>C
NM_001159287.1:c.*221T>C	NP_001152759.1:n.*221T>C
NM_001258026.1:c.*221T>C	NP_001244955.1:n.*221T>C
XR_002957378.1:n.1979T>C
NM_000365.6:c.*221T>C MANE Select	NP_000356.1:n.*221T>C
NM_001258026.2:c.*221T>C	NP_001244955.1:n.*221T>C