Canonical Allele Identifier: CA2617922836

Gene: GYS2

Linked Data

• gnomAD v4: 12-21546507-AAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21546510_21546512del , CM000674.2:g.21546510_21546512del	GRCh38
NC_000012.11:g.21699444_21699446del , CM000674.1:g.21699444_21699446del	GRCh37
NC_000012.10:g.21590711_21590713del	NCBI36
NG_016167.1:g.63338_63340del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1423-40_1423-38del MANE Select	ENSP00000261195.2:n.1423-40_1423-38del
ENST00000647960.1:c.*1425-40_*1425-38del	ENSP00000497202.1:n.*1425-40_*1425-38del
ENST00000261195.2:c.1423-40_1423-38del	ENSP00000261195.2:n.1423-40_1423-38del
NM_021957.3:c.1423-40_1423-38del	NP_068776.2:n.1423-40_1423-38del
XM_005253352.1:c.1423-40_1423-38del	XP_005253409.1:n.1423-40_1423-38del
XM_005253354.2:c.1204-40_1204-38del	XP_005253411.1:n.1204-40_1204-38del
XM_006719062.2:c.1423-40_1423-38del	XP_006719125.1:n.1423-40_1423-38del
XM_006719063.2:c.1192-40_1192-38del	XP_006719126.1:n.1192-40_1192-38del
NM_021957.4:c.1423-40_1423-38del MANE Select	NP_068776.2:n.1423-40_1423-38del
XM_006719063.3:c.1192-40_1192-38del	XP_006719126.1:n.1192-40_1192-38del
XM_024448960.1:c.1423-40_1423-38del	XP_024304728.1:n.1423-40_1423-38del