Canonical Allele Identifier: CA2617355900

Gene: TPI1

Linked Data

• gnomAD v4: 12-6870603-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870603G>C , CM000674.2:g.6870603G>C	GRCh38
NC_000012.11:g.6979767G>C , CM000674.1:g.6979767G>C	GRCh37
NC_000012.10:g.6850028G>C	NCBI36
NG_011948.1:g.8184G>C
NG_013308.1:g.7755C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*220G>C MANE Select	ENSP00000379933.4:n.*220G>C
ENST00000229270.8:c.*220G>C	ENSP00000229270.4:n.*220G>C
ENST00000396705.9:c.*220G>C	ENSP00000379933.4:n.*220G>C
ENST00000535434.5:c.*220G>C	ENSP00000443599.1:n.*220G>C
ENST00000613953.4:c.*220G>C	ENSP00000484435.1:n.*220G>C
NM_000365.5:c.*220G>C	NP_000356.1:n.*220G>C
NM_001159287.1:c.*220G>C	NP_001152759.1:n.*220G>C
NM_001258026.1:c.*220G>C	NP_001244955.1:n.*220G>C
XR_002957378.1:n.1978G>C
NM_000365.6:c.*220G>C MANE Select	NP_000356.1:n.*220G>C
NM_001258026.2:c.*220G>C	NP_001244955.1:n.*220G>C