Canonical Allele Identifier: CA603133014

Gene: TPI1

Linked Data

• dbSNP Id: rs1555132682
• gnomAD v2: 12-6979581-C-T
• gnomAD v4: 12-6870417-C-T
• MyVariant Identifiers: chr12:g.6979581C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870417C>T , CM000674.2:g.6870417C>T	GRCh38
NC_000012.11:g.6979581C>T , CM000674.1:g.6979581C>T	GRCh37
NC_000012.10:g.6849842C>T	NCBI36
NG_011948.1:g.7998C>T
NG_013308.1:g.7941G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*34C>T MANE Select	ENSP00000379933.4:n.*34C>T
ENST00000229270.8:c.*34C>T	ENSP00000229270.4:n.*34C>T
ENST00000396705.9:c.*34C>T	ENSP00000379933.4:n.*34C>T
ENST00000474253.1:n.273C>T
ENST00000535434.5:c.*34C>T	ENSP00000443599.1:n.*34C>T
ENST00000613953.4:c.*34C>T	ENSP00000484435.1:n.*34C>T
NM_000365.5:c.*34C>T	NP_000356.1:n.*34C>T
NM_001159287.1:c.*34C>T	NP_001152759.1:n.*34C>T
NM_001258026.1:c.*34C>T	NP_001244955.1:n.*34C>T
XR_002957378.1:n.1792C>T
NM_000365.6:c.*34C>T MANE Select	NP_000356.1:n.*34C>T
NM_001258026.2:c.*34C>T	NP_001244955.1:n.*34C>T