Canonical Allele Identifier: CA2617923655
Gene: GYS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21563120_21563121insC , CM000674.2:g.21563120_21563121insC GRCh38
NC_000012.11:g.21716054_21716055insC , CM000674.1:g.21716054_21716055insC GRCh37
NC_000012.10:g.21607321_21607322insC NCBI36
NG_016167.1:g.46727_46728insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261195.3:c.942-83_942-82insG MANE Select ENSP00000261195.2:n.942-83_942-82insG
ENST00000647960.1:c.*944-83_*944-82insG ENSP00000497202.1:n.*944-83_*944-82insG
ENST00000648372.1:n.869-83_869-82insG
ENST00000261195.2:c.942-83_942-82insG ENSP00000261195.2:n.942-83_942-82insG
NM_021957.3:c.942-83_942-82insG NP_068776.2:n.942-83_942-82insG
XM_005253352.1:c.942-83_942-82insG XP_005253409.1:n.942-83_942-82insG
XM_005253354.2:c.723-83_723-82insG XP_005253411.1:n.723-83_723-82insG
XM_006719062.2:c.942-83_942-82insG XP_006719125.1:n.942-83_942-82insG
XM_006719063.2:c.711-83_711-82insG XP_006719126.1:n.711-83_711-82insG
NM_021957.4:c.942-83_942-82insG MANE Select NP_068776.2:n.942-83_942-82insG
XM_006719063.3:c.711-83_711-82insG XP_006719126.1:n.711-83_711-82insG
XM_017019245.2:c.942-83_942-82insG XP_016874734.1:n.942-83_942-82insG
XM_024448960.1:c.942-83_942-82insG XP_024304728.1:n.942-83_942-82insG