Canonical Allele Identifier: CA478165602

Gene: TPI1

Linked Data

• MyVariant Identifiers: chr12:g.6979436G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870272G>C , CM000674.2:g.6870272G>C	GRCh38
NC_000012.11:g.6979436G>C , CM000674.1:g.6979436G>C	GRCh37
NC_000012.10:g.6849697G>C	NCBI36
NG_011948.1:g.7853G>C
NG_013308.1:g.8086C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396705.10:c.639G>C MANE Select	ENSP00000379933.4:p.Val213=
ENST00000229270.8:c.750G>C	ENSP00000229270.4:p.Val250=
ENST00000396705.9:c.639G>C	ENSP00000379933.4:p.Val213=
ENST00000474253.1:n.128G>C
ENST00000488464.6:c.393G>C	ENSP00000475620.1:p.Val131=
ENST00000535434.5:c.393G>C	ENSP00000443599.1:p.Val131=
ENST00000613953.4:c.750G>C	ENSP00000484435.1:p.Val250=
NM_000365.5:c.639G>C	NP_000356.1:p.Val213=
NM_001159287.1:c.750G>C	NP_001152759.1:p.Val250=
NM_001258026.1:c.393G>C	NP_001244955.1:p.Val131=
XR_002957378.1:n.1647G>C
NM_000365.6:c.639G>C MANE Select	NP_000356.1:p.Val213=
NM_001258026.2:c.393G>C	NP_001244955.1:p.Val131=