Canonical Allele Identifier: CA945500259

Gene: GYS2

Linked Data

• gnomAD v3: 12-21562720-AAGATG-A
• gnomAD v4: 12-21562720-AAGATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21562722_21562726del , CM000674.2:g.21562722_21562726del	GRCh38
NC_000012.11:g.21715656_21715660del , CM000674.1:g.21715656_21715660del	GRCh37
NC_000012.10:g.21606923_21606927del	NCBI36
NG_016167.1:g.47123_47127del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1062+193_1062+197del MANE Select	ENSP00000261195.2:n.1062+193_1062+197del
ENST00000647960.1:c.*1064+193_*1064+197del	ENSP00000497202.1:n.*1064+193_*1064+197del
ENST00000648372.1:n.989+193_989+197del
ENST00000261195.2:c.1062+193_1062+197del	ENSP00000261195.2:n.1062+193_1062+197del
NM_021957.3:c.1062+193_1062+197del	NP_068776.2:n.1062+193_1062+197del
XM_005253352.1:c.1062+193_1062+197del	XP_005253409.1:n.1062+193_1062+197del
XM_005253354.2:c.843+193_843+197del	XP_005253411.1:n.843+193_843+197del
XM_006719062.2:c.1062+193_1062+197del	XP_006719125.1:n.1062+193_1062+197del
XM_006719063.2:c.831+193_831+197del	XP_006719126.1:n.831+193_831+197del
NM_021957.4:c.1062+193_1062+197del MANE Select	NP_068776.2:n.1062+193_1062+197del
XM_006719063.3:c.831+193_831+197del	XP_006719126.1:n.831+193_831+197del
XM_017019245.2:c.1062+193_1062+197del	XP_016874734.1:n.1062+193_1062+197del
XM_024448960.1:c.1062+193_1062+197del	XP_024304728.1:n.1062+193_1062+197del