Canonical Allele Identifier: CA1788918773

Gene: GGH

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63028658T= , CM000670.2:g.63028658T=	GRCh38
NC_000008.10:g.63941217T= , CM000670.1:g.63941217T=	GRCh37
NC_000008.9:g.64103771T=	NCBI36
NG_028126.1:g.15394A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260118.7:c.276-1393A= MANE Select	ENSP00000260118.6:n.276-1393A=
ENST00000518113.2:c.276-1393A=	ENSP00000504520.1:n.276-1393A=
ENST00000518466.6:n.239-1393A=
ENST00000523788.2:n.1811A=
ENST00000677327.1:n.915-1393A=
ENST00000677459.1:c.*191-1393A=	ENSP00000503731.1:n.*191-1393A=
ENST00000677482.1:c.276-1393A=	ENSP00000504590.1:n.276-1393A=
ENST00000678045.1:n.1231-1393A=
ENST00000678069.1:n.1818A=
ENST00000679326.1:c.276-1393A=	ENSP00000504262.1:n.276-1393A=
ENST00000260118.6:c.276-1393A=	ENSP00000260118.6:n.276-1393A=
ENST00000518113.1:n.51-1393A=
ENST00000518966.5:n.309-1393A=
ENST00000520609.5:n.309-1393A=
NM_003878.2:c.276-1393A=	NP_003869.1:n.276-1393A=
XM_011517623.1:c.276-1393A=	XP_011515925.1:n.276-1393A=
XM_011517623.3:c.276-1393A=	XP_011515925.1:n.276-1393A=
NM_003878.3:c.276-1393A= MANE Select	NP_003869.1:n.276-1393A=