Canonical Allele Identifier: CA362838464

Gene: TPMT

Linked Data

• MyVariant Identifiers: chr6:g.18143930C>A (hg19) ; chr6:g.18143699C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18143699C>A , CM000668.2:g.18143699C>A	GRCh38
NC_000006.11:g.18143930C>A , CM000668.1:g.18143930C>A	GRCh37
NC_000006.10:g.18251909C>A	NCBI36
NG_012137.2:g.16445G>T
NG_012137.3:g.16445G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.263G>T MANE Select	ENSP00000312304.4:p.Gly88Val
ENST00000309983.4:c.263G>T	ENSP00000312304.4:p.Gly88Val
NM_000367.3:c.263G>T	NP_000358.1:p.Gly88Val
XM_011514839.1:c.263G>T	XP_011513141.1:p.Gly88Val
XM_011514840.1:c.194G>T	XP_011513142.1:p.Gly65Val
NM_000367.4:c.263G>T	NP_000358.1:p.Gly88Val
NM_001346817.1:c.263G>T	NP_001333746.1:p.Gly88Val
NM_001346818.1:c.263G>T	NP_001333747.1:p.Gly88Val
NM_000367.5:c.263G>T MANE Select	NP_000358.1:p.Gly88Val