Canonical Allele Identifier: CA10154368

Gene: GGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24620344G>A , CM000684.2:g.24620344G>A	GRCh38
NC_000022.10:g.25016311G>A , CM000684.1:g.25016311G>A	GRCh37
NC_000022.9:g.23346311G>A	NCBI36
NG_008111.1:g.41594G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400382.6:c.399G>A MANE Select	ENSP00000383232.1:p.Ala133=
ENST00000651180.1:n.886G>A
ENST00000652248.1:c.*889G>A	ENSP00000499210.1:n.*889G>A
ENST00000248923.8:c.399G>A	ENSP00000248923.4:p.Ala133=
ENST00000400380.5:c.399G>A	ENSP00000383231.1:p.Ala133=
ENST00000400382.5:c.399G>A	ENSP00000383232.1:p.Ala133=
ENST00000412658.5:c.399G>A	ENSP00000393537.1:p.Ala133=
ENST00000419133.5:c.399G>A	ENSP00000395271.1:p.Ala133=
ENST00000425895.5:c.399G>A	ENSP00000387499.1:p.Ala133=
ENST00000487766.1:n.149G>A
NM_001288833.1:c.399G>A	NP_001275762.1:p.Ala133=
NM_013421.2:c.399G>A	NP_038265.2:p.Ala133=
NM_013430.2:c.399G>A	NP_038347.2:p.Ala133=
NM_001288833.2:c.399G>A MANE Select	NP_001275762.1:p.Ala133=
NM_013421.3:c.399G>A	NP_038265.2:p.Ala133=
NM_013430.3:c.399G>A	NP_038347.2:p.Ala133=