Canonical Allele Identifier: CA10154489

Gene: GGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24623225C>T , CM000684.2:g.24623225C>T	GRCh38
NC_000022.10:g.25019192C>T , CM000684.1:g.25019192C>T	GRCh37
NC_000022.9:g.23349192C>T	NCBI36
NG_008111.1:g.44475C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400382.6:c.852C>T MANE Select	ENSP00000383232.1:p.Pro284=
ENST00000651180.1:n.1339C>T
ENST00000652248.1:c.*1342C>T	ENSP00000499210.1:n.*1342C>T
ENST00000248923.8:c.852C>T	ENSP00000248923.4:p.Pro284=
ENST00000400380.5:c.852C>T	ENSP00000383231.1:p.Pro284=
ENST00000400382.5:c.852C>T	ENSP00000383232.1:p.Pro284=
ENST00000412658.5:c.852C>T	ENSP00000393537.1:p.Pro284=
ENST00000425895.5:c.852C>T	ENSP00000387499.1:p.Pro284=
ENST00000466310.5:n.232C>T
NM_001288833.1:c.852C>T	NP_001275762.1:p.Pro284=
NM_013421.2:c.852C>T	NP_038265.2:p.Pro284=
NM_013430.2:c.852C>T	NP_038347.2:p.Pro284=
NM_001288833.2:c.852C>T MANE Select	NP_001275762.1:p.Pro284=
NM_013421.3:c.852C>T	NP_038265.2:p.Pro284=
NM_013430.3:c.852C>T	NP_038347.2:p.Pro284=