Canonical Allele Identifier: CA1788923340

Gene: GGH

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63038753A= , CM000670.2:g.63038753A=	GRCh38
NC_000008.10:g.63951312A= , CM000670.1:g.63951312A=	GRCh37
NC_000008.9:g.64113866A=	NCBI36
NG_028126.1:g.5299T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003878.3:c.16T= MANE Select	NP_003869.1:p.Cys6=
ENST00000260118.7:c.16T= MANE Select	ENSP00000260118.6:p.Cys6=
NM_003878.2:c.16T=	NP_003869.1:p.Cys6=
ENST00000260118.6:c.16T=	ENSP00000260118.6:p.Cys6=
ENST00000518113.2:c.16T=	ENSP00000504520.1:p.Cys6=
ENST00000518966.5:n.49T=
ENST00000520609.5:n.49T=
ENST00000523788.1:n.50T=
ENST00000523788.2:n.43T=
ENST00000677327.1:n.655T=
ENST00000677459.1:c.16T=	ENSP00000503731.1:p.Cys6=
ENST00000677482.1:c.16T=	ENSP00000504590.1:p.Cys6=
ENST00000678069.1:n.50T=
ENST00000679326.1:c.16T=	ENSP00000504262.1:p.Cys6=
XM_011517623.1:c.16T=	XP_011515925.1:p.Cys6=
XM_011517623.3:c.16T=	XP_011515925.1:p.Cys6=