Canonical Allele Identifier: CA322691188

Gene: GGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24627703C>T , CM000684.2:g.24627703C>T	GRCh38
NC_000022.10:g.25023670C>T , CM000684.1:g.25023670C>T	GRCh37
NC_000022.9:g.23353670C>T	NCBI36
NG_008111.1:g.48953C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400382.6:c.1208+84C>T MANE Select	ENSP00000383232.1:n.1208+84C>T
ENST00000651180.1:n.1695+84C>T
ENST00000652248.1:c.*1720+84C>T	ENSP00000499210.1:n.*1720+84C>T
ENST00000248923.8:c.1208+84C>T	ENSP00000248923.4:n.1208+84C>T
ENST00000400380.5:c.1208+84C>T	ENSP00000383231.1:n.1208+84C>T
ENST00000400382.5:c.1208+84C>T	ENSP00000383232.1:n.1208+84C>T
ENST00000401885.5:c.176+84C>T	ENSP00000384381.1:n.176+84C>T
ENST00000403838.5:c.176+84C>T	ENSP00000384820.1:n.176+84C>T
ENST00000404223.5:c.176+84C>T	ENSP00000385016.1:n.176+84C>T
ENST00000404532.5:c.176+84C>T	ENSP00000385445.1:n.176+84C>T
ENST00000404920.1:c.176+84C>T	ENSP00000385001.1:n.176+84C>T
ENST00000412658.5:c.1208+84C>T	ENSP00000393537.1:n.1208+84C>T
ENST00000425895.5:c.*129+84C>T	ENSP00000387499.1:n.*129+84C>T
ENST00000466310.5:n.610+84C>T
NM_001288833.1:c.1208+84C>T	NP_001275762.1:n.1208+84C>T
NM_013421.2:c.1208+84C>T	NP_038265.2:n.1208+84C>T
NM_013430.2:c.1208+84C>T	NP_038347.2:n.1208+84C>T
NM_001288833.2:c.1208+84C>T MANE Select	NP_001275762.1:n.1208+84C>T
NM_013421.3:c.1208+84C>T	NP_038265.2:n.1208+84C>T
NM_013430.3:c.1208+84C>T	NP_038347.2:n.1208+84C>T