Canonical Allele Identifier: CA2021178857

Gene: GYS2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21562976G= , CM000674.2:g.21562976G=	GRCh38
NC_000012.11:g.21715910G= , CM000674.1:g.21715910G=	GRCh37
NC_000012.10:g.21607177G=	NCBI36
NG_016167.1:g.46872C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1004C= MANE Select	ENSP00000261195.2:p.Ser335=
ENST00000647960.1:c.*1006C=	ENSP00000497202.1:n.*1006C=
ENST00000648372.1:n.931C=
ENST00000261195.2:c.1004C=	ENSP00000261195.2:p.Ser335=
NM_021957.3:c.1004C=	NP_068776.2:p.Ser335=
XM_005253352.1:c.1004C=	XP_005253409.1:p.Ser335=
XM_005253354.2:c.785C=	XP_005253411.1:p.Ser262=
XM_006719062.2:c.1004C=	XP_006719125.1:p.Ser335=
XM_006719063.2:c.773C=	XP_006719126.1:p.Ser258=
NM_021957.4:c.1004C= MANE Select	NP_068776.2:p.Ser335=
XM_006719063.3:c.773C=	XP_006719126.1:p.Ser258=
XM_017019245.2:c.1004C=	XP_016874734.1:p.Ser335=
XM_024448960.1:c.1004C=	XP_024304728.1:p.Ser335=