Canonical Allele Identifier: CA2021167134
Gene: GYS2 HGNC NCBI

Linked Data

dbSNP Id: rs1944042030

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21546508_21546509insTGAT , CM000674.2:g.21546508_21546509insTGAT GRCh38
NC_000012.11:g.21699442_21699443insTGAT , CM000674.1:g.21699442_21699443insTGAT GRCh37
NC_000012.10:g.21590709_21590710insTGAT NCBI36
NG_016167.1:g.63339_63340insATCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.1423-39_1423-38insATCA MANE Select ENSP00000261195.2:n.1423-39_1423-38insATCA
ENST00000647960.1:c.*1425-39_*1425-38insATCA ENSP00000497202.1:n.*1425-39_*1425-38insATCA
ENST00000261195.2:c.1423-39_1423-38insATCA ENSP00000261195.2:n.1423-39_1423-38insATCA
NM_021957.3:c.1423-39_1423-38insATCA NP_068776.2:n.1423-39_1423-38insATCA
XM_005253352.1:c.1423-39_1423-38insATCA XP_005253409.1:n.1423-39_1423-38insATCA
XM_005253354.2:c.1204-39_1204-38insATCA XP_005253411.1:n.1204-39_1204-38insATCA
XM_006719062.2:c.1423-39_1423-38insATCA XP_006719125.1:n.1423-39_1423-38insATCA
XM_006719063.2:c.1192-39_1192-38insATCA XP_006719126.1:n.1192-39_1192-38insATCA
NM_021957.4:c.1423-39_1423-38insATCA MANE Select NP_068776.2:n.1423-39_1423-38insATCA
XM_006719063.3:c.1192-39_1192-38insATCA XP_006719126.1:n.1192-39_1192-38insATCA
XM_024448960.1:c.1423-39_1423-38insATCA XP_024304728.1:n.1423-39_1423-38insATCA