Canonical Allele Identifier: CA2021178575

Gene: GYS2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21562719_21562724delinsAAAGAT , CM000674.2:g.21562719_21562724delinsAAAGAT	GRCh38
NC_000012.11:g.21715653_21715658delinsAAAGAT , CM000674.1:g.21715653_21715658delinsAAAGAT	GRCh37
NC_000012.10:g.21606920_21606925delinsAAAGAT	NCBI36
NG_016167.1:g.47124_47129delinsATCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261195.3:c.1062+194_1062+199delinsATCTTT MANE Select	ENSP00000261195.2:n.1062+194_1062+199delinsATCTTT
ENST00000647960.1:c.*1064+194_*1064+199delinsATCTTT	ENSP00000497202.1:n.*1064+194_*1064+199delinsATCTTT
ENST00000648372.1:n.989+194_989+199delinsATCTTT
ENST00000261195.2:c.1062+194_1062+199delinsATCTTT	ENSP00000261195.2:n.1062+194_1062+199delinsATCTTT
NM_021957.3:c.1062+194_1062+199delinsATCTTT	NP_068776.2:n.1062+194_1062+199delinsATCTTT
XM_005253352.1:c.1062+194_1062+199delinsATCTTT	XP_005253409.1:n.1062+194_1062+199delinsATCTTT
XM_005253354.2:c.843+194_843+199delinsATCTTT	XP_005253411.1:n.843+194_843+199delinsATCTTT
XM_006719062.2:c.1062+194_1062+199delinsATCTTT	XP_006719125.1:n.1062+194_1062+199delinsATCTTT
XM_006719063.2:c.831+194_831+199delinsATCTTT	XP_006719126.1:n.831+194_831+199delinsATCTTT
NM_021957.4:c.1062+194_1062+199delinsATCTTT MANE Select	NP_068776.2:n.1062+194_1062+199delinsATCTTT
XM_006719063.3:c.831+194_831+199delinsATCTTT	XP_006719126.1:n.831+194_831+199delinsATCTTT
XM_017019245.2:c.1062+194_1062+199delinsATCTTT	XP_016874734.1:n.1062+194_1062+199delinsATCTTT
XM_024448960.1:c.1062+194_1062+199delinsATCTTT	XP_024304728.1:n.1062+194_1062+199delinsATCTTT