Canonical Allele Identifier: CA1613557356

Gene: TPMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.18138813_18138817delinsAAGCT , CM000668.2:g.18138813_18138817delinsAAGCT	GRCh38
NC_000006.11:g.18139044_18139048delinsAAGCT , CM000668.1:g.18139044_18139048delinsAAGCT	GRCh37
NC_000006.10:g.18247023_18247027delinsAAGCT	NCBI36
NG_012137.2:g.21327_21331delinsAGCTT
NG_012137.3:g.21327_21331delinsAGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309983.5:c.494+146_494+150delinsAGCTT MANE Select	ENSP00000312304.4:n.494+146_494+150delinsAGCTT
ENST00000309983.4:c.494+146_494+150delinsAGCTT	ENSP00000312304.4:n.494+146_494+150delinsAGCTT
NM_000367.3:c.494+146_494+150delinsAGCTT	NP_000358.1:n.494+146_494+150delinsAGCTT
XM_011514839.1:c.494+146_494+150delinsAGCTT	XP_011513141.1:n.494+146_494+150delinsAGCTT
XM_011514840.1:c.425+146_425+150delinsAGCTT	XP_011513142.1:n.425+146_425+150delinsAGCTT
NM_000367.4:c.494+146_494+150delinsAGCTT	NP_000358.1:n.494+146_494+150delinsAGCTT
NM_001346817.1:c.494+146_494+150delinsAGCTT	NP_001333746.1:n.494+146_494+150delinsAGCTT
NM_001346818.1:c.494+146_494+150delinsAGCTT	NP_001333747.1:n.494+146_494+150delinsAGCTT
NM_000367.5:c.494+146_494+150delinsAGCTT MANE Select	NP_000358.1:n.494+146_494+150delinsAGCTT