Canonical Allele Identifier: CA2021163295

Gene: GYS2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21542503A= , CM000674.2:g.21542503A=	GRCh38
NC_000012.11:g.21695437A= , CM000674.1:g.21695437A=	GRCh37
NC_000012.10:g.21586704A=	NCBI36
NG_016167.1:g.67345T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261195.3:c.1638T= MANE Select	ENSP00000261195.2:p.Thr546=
ENST00000647960.1:c.*1640T=	ENSP00000497202.1:n.*1640T=
ENST00000261195.2:c.1638T=	ENSP00000261195.2:p.Thr546=
NM_021957.3:c.1638T=	NP_068776.2:p.Thr546=
XM_005253352.1:c.1638T=	XP_005253409.1:p.Thr546=
XM_005253354.2:c.1419T=	XP_005253411.1:p.Thr473=
XM_006719062.2:c.1638T=	XP_006719125.1:p.Thr546=
XM_006719063.2:c.1407T=	XP_006719126.1:p.Thr469=
NM_021957.4:c.1638T= MANE Select	NP_068776.2:p.Thr546=
XM_006719063.3:c.1407T=	XP_006719126.1:p.Thr469=
XM_024448960.1:c.1638T=	XP_024304728.1:p.Thr546=