Canonical Allele Identifier: CA603133008

Gene: TPI1

Linked Data

• dbSNP Id: rs1555132657
• gnomAD v2: 12-6979553-A-G
• gnomAD v3: 12-6870389-A-G
• gnomAD v4: 12-6870389-A-G
• MyVariant Identifiers: chr12:g.6979553A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870389A>G , CM000674.2:g.6870389A>G	GRCh38
NC_000012.11:g.6979553A>G , CM000674.1:g.6979553A>G	GRCh37
NC_000012.10:g.6849814A>G	NCBI36
NG_011948.1:g.7970A>G
NG_013308.1:g.7969T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.*6A>G MANE Select	ENSP00000379933.4:n.*6A>G
ENST00000229270.8:c.*6A>G	ENSP00000229270.4:n.*6A>G
ENST00000396705.9:c.*6A>G	ENSP00000379933.4:n.*6A>G
ENST00000474253.1:n.245A>G
ENST00000535434.5:c.*6A>G	ENSP00000443599.1:n.*6A>G
ENST00000613953.4:c.*6A>G	ENSP00000484435.1:n.*6A>G
NM_000365.5:c.*6A>G	NP_000356.1:n.*6A>G
NM_001159287.1:c.*6A>G	NP_001152759.1:n.*6A>G
NM_001258026.1:c.*6A>G	NP_001244955.1:n.*6A>G
XR_002957378.1:n.1764A>G
NM_000365.6:c.*6A>G MANE Select	NP_000356.1:n.*6A>G
NM_001258026.2:c.*6A>G	NP_001244955.1:n.*6A>G