Canonical Allele Identifier: CA1630835172

Gene: GGH

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63026205G= , CM000670.2:g.63026205G=	GRCh38
NC_000008.10:g.63938764G= , CM000670.1:g.63938764G=	GRCh37
NC_000008.9:g.64101318G=	NCBI36
NG_028126.1:g.17847C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003878.3:c.452C= MANE Select	NP_003869.1:p.Thr151=
ENST00000260118.7:c.452C= MANE Select	ENSP00000260118.6:p.Thr151=
NM_003878.2:c.452C=	NP_003869.1:p.Thr151=
ENST00000260118.6:c.452C=	ENSP00000260118.6:p.Thr151=
ENST00000518113.1:n.227C=
ENST00000518113.2:c.452C=	ENSP00000504520.1:p.Thr151=
ENST00000518466.5:n.29C=
ENST00000518466.6:n.415C=
ENST00000520609.5:n.485C=
ENST00000523788.2:n.4264C=
ENST00000677327.1:n.1091C=
ENST00000677459.1:c.*367C=	ENSP00000503731.1:n.*367C=
ENST00000677482.1:c.452C=	ENSP00000504590.1:p.Thr151=
ENST00000677919.1:c.29C=	ENSP00000504579.1:p.Thr10=
ENST00000678045.1:n.1407C=
ENST00000678069.1:n.3387C=
ENST00000679326.1:c.452C=	ENSP00000504262.1:p.Thr151=
XM_011517623.1:c.452C=	XP_011515925.1:p.Thr151=
XM_011517623.3:c.452C=	XP_011515925.1:p.Thr151=