Canonical Allele Identifier: CA2646987789

Gene: GSTM3 GSTM5

Linked Data

• gnomAD v4: 1-109737172-G-GAAAGGAAAATACACCAAATCTTATAACGACCCCAACCCAGTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109737174_109737217dup , CM000663.2:g.109737174_109737217dup	GRCh38
NC_000001.10:g.110279796_110279839dup , CM000663.1:g.110279796_110279839dup	GRCh37
NC_000001.9:g.110081319_110081362dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361066.7:c.580-47_580-4dup (GSTM3) MANE Select	ENSP00000354357.2:n.580-47_580-4dup
ENST00000256594.7:c.580-47_580-4dup (GSTM3)	ENSP00000256594.3:n.580-47_580-4dup
ENST00000361066.6:c.580-47_580-4dup (GSTM3)	ENSP00000354357.2:n.580-47_580-4dup
ENST00000429410.2:n.82+24826_82+24869dup (GSTM5)
ENST00000476321.5:n.501_544dup (GSTM3)
ENST00000486823.5:n.544-47_544-4dup (GSTM3)
ENST00000488824.1:n.925-47_925-4dup (GSTM3)
NM_000849.4:c.580-47_580-4dup (GSTM3)	NP_000840.2:n.580-47_580-4dup
NR_024537.1:n.814-47_814-4dup (GSTM3)
XM_011541296.1:c.799-47_799-4dup (GSTM3)	XP_011539598.1:n.799-47_799-4dup
NM_000849.5:c.580-47_580-4dup (GSTM3) MANE Select	NP_000840.2:n.580-47_580-4dup
NR_024537.2:n.814-47_814-4dup (GSTM3)