Canonical Allele Identifier: CA478165718

Gene: TPI1

Linked Data

• dbSNP Id: rs2138095406
• gnomAD v4: 12-6870311-T-C
• MyVariant Identifiers: chr12:g.6979475T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870311T>C , CM000674.2:g.6870311T>C	GRCh38
NC_000012.11:g.6979475T>C , CM000674.1:g.6979475T>C	GRCh37
NC_000012.10:g.6849736T>C	NCBI36
NG_011948.1:g.7892T>C
NG_013308.1:g.8047A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.678T>C MANE Select	ENSP00000379933.4:p.Asp226=
ENST00000229270.8:c.789T>C	ENSP00000229270.4:p.Asp263=
ENST00000396705.9:c.678T>C	ENSP00000379933.4:p.Asp226=
ENST00000474253.1:n.167T>C
ENST00000488464.6:c.432T>C	ENSP00000475620.1:p.Asp144=
ENST00000535434.5:c.432T>C	ENSP00000443599.1:p.Asp144=
ENST00000613953.4:c.789T>C	ENSP00000484435.1:p.Asp263=
NM_000365.5:c.678T>C	NP_000356.1:p.Asp226=
NM_001159287.1:c.789T>C	NP_001152759.1:p.Asp263=
NM_001258026.1:c.432T>C	NP_001244955.1:p.Asp144=
XR_002957378.1:n.1686T>C
NM_000365.6:c.678T>C MANE Select	NP_000356.1:p.Asp226=
NM_001258026.2:c.432T>C	NP_001244955.1:p.Asp144=