Canonical Allele Identifier: CA383714151

Gene: TPI1

Linked Data

• dbSNP Id: rs1555132634
• gnomAD v2: 12-6979521-G-A
• gnomAD v4: 12-6870357-G-A
• COSMIC: COSM3955098 ; COSM3955099
• MyVariant Identifiers: chr12:g.6979521G>A (hg19) ; chr12:g.6870357G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6870357G>A , CM000674.2:g.6870357G>A	GRCh38
NC_000012.11:g.6979521G>A , CM000674.1:g.6979521G>A	GRCh37
NC_000012.10:g.6849782G>A	NCBI36
NG_011948.1:g.7938G>A
NG_013308.1:g.8001C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396705.10:c.724G>A MANE Select	ENSP00000379933.4:p.Val242Met
ENST00000229270.8:c.835G>A	ENSP00000229270.4:p.Val279Met
ENST00000396705.9:c.724G>A	ENSP00000379933.4:p.Val242Met
ENST00000474253.1:n.213G>A
ENST00000488464.6:c.478G>A	ENSP00000475620.1:p.Val160Met
ENST00000535434.5:c.478G>A	ENSP00000443599.1:p.Val160Met
ENST00000613953.4:c.835G>A	ENSP00000484435.1:p.Val279Met
NM_000365.5:c.724G>A	NP_000356.1:p.Val242Met
NM_001159287.1:c.835G>A	NP_001152759.1:p.Val279Met
NM_001258026.1:c.478G>A	NP_001244955.1:p.Val160Met
XR_002957378.1:n.1732G>A
NM_000365.6:c.724G>A MANE Select	NP_000356.1:p.Val242Met
NM_001258026.2:c.478G>A	NP_001244955.1:p.Val160Met