Canonical Allele Identifier: CA362832738

Gene: TPMT

Linked Data

• MyVariant Identifiers: chr6:g.18131000T>G (hg19) ; chr6:g.18130769T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18130769T>G , CM000668.2:g.18130769T>G	GRCh38
NC_000006.11:g.18131000T>G , CM000668.1:g.18131000T>G	GRCh37
NC_000006.10:g.18238979T>G	NCBI36
NG_012137.2:g.29375A>C
NG_012137.3:g.29375A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309983.5:c.637A>C MANE Select	ENSP00000312304.4:p.Asn213His
ENST00000309983.4:c.637A>C	ENSP00000312304.4:p.Asn213His
NM_000367.3:c.637A>C	NP_000358.1:p.Asn213His
XM_011514839.1:c.592A>C	XP_011513141.1:p.Asn198His
XM_011514840.1:c.568A>C	XP_011513142.1:p.Asn190His
NM_000367.4:c.637A>C	NP_000358.1:p.Asn213His
NM_001346817.1:c.637A>C	NP_001333746.1:p.Asn213His
NM_001346818.1:c.592A>C	NP_001333747.1:p.Asn198His
NM_000367.5:c.637A>C MANE Select	NP_000358.1:p.Asn213His