Canonical Allele Identifier: CA603133043

Gene: TPI1

Linked Data

• dbSNP Id: rs1555132871
• gnomAD v2: 12-6979830-C-G
• MyVariant Identifiers: chr12:g.6979830C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870666C>G , CM000674.2:g.6870666C>G	GRCh38
NC_000012.11:g.6979830C>G , CM000674.1:g.6979830C>G	GRCh37
NC_000012.10:g.6850091C>G	NCBI36
NG_011948.1:g.8247C>G
NG_013308.1:g.7692G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*283C>G MANE Select	ENSP00000379933.4:n.*283C>G
ENST00000229270.8:c.*283C>G	ENSP00000229270.4:n.*283C>G
ENST00000396705.9:c.*283C>G	ENSP00000379933.4:n.*283C>G
ENST00000535434.5:c.*283C>G	ENSP00000443599.1:n.*283C>G
ENST00000613953.4:c.*283C>G	ENSP00000484435.1:n.*283C>G
NM_000365.5:c.*283C>G	NP_000356.1:n.*283C>G
NM_001159287.1:c.*283C>G	NP_001152759.1:n.*283C>G
NM_001258026.1:c.*283C>G	NP_001244955.1:n.*283C>G
XR_002957378.1:n.2041C>G
NM_000365.6:c.*283C>G MANE Select	NP_000356.1:n.*283C>G
NM_001258026.2:c.*283C>G	NP_001244955.1:n.*283C>G