Canonical Allele Identifier: CA2569420318

Gene: GYS2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21562719A>T , CM000674.2:g.21562719A>T	GRCh38
NC_000012.11:g.21715653A>T , CM000674.1:g.21715653A>T	GRCh37
NC_000012.10:g.21606920A>T	NCBI36
NG_016167.1:g.47129T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1062+199T>A MANE Select	ENSP00000261195.2:n.1062+199T>A
ENST00000647960.1:c.*1064+199T>A	ENSP00000497202.1:n.*1064+199T>A
ENST00000648372.1:n.989+199T>A
ENST00000261195.2:c.1062+199T>A	ENSP00000261195.2:n.1062+199T>A
NM_021957.3:c.1062+199T>A	NP_068776.2:n.1062+199T>A
XM_005253352.1:c.1062+199T>A	XP_005253409.1:n.1062+199T>A
XM_005253354.2:c.843+199T>A	XP_005253411.1:n.843+199T>A
XM_006719062.2:c.1062+199T>A	XP_006719125.1:n.1062+199T>A
XM_006719063.2:c.831+199T>A	XP_006719126.1:n.831+199T>A
NM_021957.4:c.1062+199T>A MANE Select	NP_068776.2:n.1062+199T>A
XM_006719063.3:c.831+199T>A	XP_006719126.1:n.831+199T>A
XM_017019245.2:c.1062+199T>A	XP_016874734.1:n.1062+199T>A
XM_024448960.1:c.1062+199T>A	XP_024304728.1:n.1062+199T>A