Canonical Allele Identifier: CA1788919487

Gene: GGH

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.63030158C= , CM000670.2:g.63030158C=	GRCh38
NC_000008.10:g.63942717C= , CM000670.1:g.63942717C=	GRCh37
NC_000008.9:g.64105271C=	NCBI36
NG_028126.1:g.13894G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003878.3:c.275+9G= MANE Select	NP_003869.1:n.275+9G=
ENST00000260118.7:c.275+9G= MANE Select	ENSP00000260118.6:n.275+9G=
NM_003878.2:c.275+9G=	NP_003869.1:n.275+9G=
ENST00000260118.6:c.275+9G=	ENSP00000260118.6:n.275+9G=
ENST00000518113.1:n.50+9G=
ENST00000518113.2:c.275+9G=	ENSP00000504520.1:n.275+9G=
ENST00000518466.6:n.238+9G=
ENST00000518966.5:n.308+9G=
ENST00000520609.5:n.308+9G=
ENST00000523788.1:n.318G=
ENST00000523788.2:n.311G=
ENST00000677327.1:n.914+9G=
ENST00000677459.1:c.*190+9G=	ENSP00000503731.1:n.*190+9G=
ENST00000677482.1:c.275+9G=	ENSP00000504590.1:n.275+9G=
ENST00000678045.1:n.1230+9G=
ENST00000678069.1:n.318G=
ENST00000679326.1:c.275+9G=	ENSP00000504262.1:n.275+9G=
XM_011517623.1:c.275+9G=	XP_011515925.1:n.275+9G=
XM_011517623.3:c.275+9G=	XP_011515925.1:n.275+9G=