Canonical Allele Identifier: CA2021177038

Gene: GYS2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21559421T= , CM000674.2:g.21559421T=	GRCh38
NC_000012.11:g.21712355T= , CM000674.1:g.21712355T=	GRCh37
NC_000012.10:g.21603622T=	NCBI36
NG_016167.1:g.50427A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1229+230A= MANE Select	ENSP00000261195.2:n.1229+230A=
ENST00000647960.1:c.*1231+230A=	ENSP00000497202.1:n.*1231+230A=
ENST00000648372.1:n.1156+230A=
ENST00000261195.2:c.1229+230A=	ENSP00000261195.2:n.1229+230A=
NM_021957.3:c.1229+230A=	NP_068776.2:n.1229+230A=
XM_005253352.1:c.1229+230A=	XP_005253409.1:n.1229+230A=
XM_005253354.2:c.1010+230A=	XP_005253411.1:n.1010+230A=
XM_006719062.2:c.1229+230A=	XP_006719125.1:n.1229+230A=
XM_006719063.2:c.998+230A=	XP_006719126.1:n.998+230A=
NM_021957.4:c.1229+230A= MANE Select	NP_068776.2:n.1229+230A=
XM_006719063.3:c.998+230A=	XP_006719126.1:n.998+230A=
XM_024448960.1:c.1229+230A=	XP_024304728.1:n.1229+230A=