Canonical Allele Identifier: CA603133004

Gene: TPI1

Linked Data

• dbSNP Id: rs1555132568
• gnomAD v2: 12-6979421-C-T
• gnomAD v3: 12-6870257-C-T
• gnomAD v4: 12-6870257-C-T
• MyVariant Identifiers: chr12:g.6979421C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870257C>T , CM000674.2:g.6870257C>T	GRCh38
NC_000012.11:g.6979421C>T , CM000674.1:g.6979421C>T	GRCh37
NC_000012.10:g.6849682C>T	NCBI36
NG_011948.1:g.7838C>T
NG_013308.1:g.8101G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396705.10:c.632-8C>T MANE Select	ENSP00000379933.4:n.632-8C>T
ENST00000229270.8:c.743-8C>T	ENSP00000229270.4:n.743-8C>T
ENST00000396705.9:c.632-8C>T	ENSP00000379933.4:n.632-8C>T
ENST00000474253.1:n.121-8C>T
ENST00000488464.6:c.386-8C>T	ENSP00000475620.1:n.386-8C>T
ENST00000535434.5:c.386-8C>T	ENSP00000443599.1:n.386-8C>T
ENST00000613953.4:c.743-8C>T	ENSP00000484435.1:n.743-8C>T
NM_000365.5:c.632-8C>T	NP_000356.1:n.632-8C>T
NM_001159287.1:c.743-8C>T	NP_001152759.1:n.743-8C>T
NM_001258026.1:c.386-8C>T	NP_001244955.1:n.386-8C>T
XR_002957378.1:n.1640-8C>T
NM_000365.6:c.632-8C>T MANE Select	NP_000356.1:n.632-8C>T
NM_001258026.2:c.386-8C>T	NP_001244955.1:n.386-8C>T