Canonical Allele Identifier: CA10154708

Gene: GGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24628109G>A , CM000684.2:g.24628109G>A	GRCh38
NC_000022.10:g.25024076G>A , CM000684.1:g.25024076G>A	GRCh37
NC_000022.9:g.23354076G>A	NCBI36
NG_008111.1:g.49359G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400382.6:c.1365G>A MANE Select	ENSP00000383232.1:p.Pro455=
ENST00000651180.1:n.1852G>A
ENST00000652248.1:c.*1877G>A	ENSP00000499210.1:n.*1877G>A
ENST00000248923.8:c.1365G>A	ENSP00000248923.4:p.Pro455=
ENST00000400380.5:c.1365G>A	ENSP00000383231.1:p.Pro455=
ENST00000400382.5:c.1365G>A	ENSP00000383232.1:p.Pro455=
ENST00000401885.5:c.333G>A	ENSP00000384381.1:p.Pro111=
ENST00000403838.5:c.333G>A	ENSP00000384820.1:p.Pro111=
ENST00000404223.5:c.333G>A	ENSP00000385016.1:p.Pro111=
ENST00000404532.5:c.333G>A	ENSP00000385445.1:p.Pro111=
ENST00000404920.1:c.333G>A	ENSP00000385001.1:p.Pro111=
ENST00000412658.5:c.1365G>A	ENSP00000393537.1:p.Pro455=
ENST00000425895.5:c.*286G>A	ENSP00000387499.1:n.*286G>A
ENST00000466310.5:n.767G>A
ENST00000490087.1:n.105-130G>A
NM_001288833.1:c.1365G>A	NP_001275762.1:p.Pro455=
NM_013421.2:c.1365G>A	NP_038265.2:p.Pro455=
NM_013430.2:c.1365G>A	NP_038347.2:p.Pro455=
NM_001288833.2:c.1365G>A MANE Select	NP_001275762.1:p.Pro455=
NM_013421.3:c.1365G>A	NP_038265.2:p.Pro455=
NM_013430.3:c.1365G>A	NP_038347.2:p.Pro455=