Canonical Allele Identifier: CA1410031537
Gene: GYG1 HGNC NCBI

Linked Data

dbSNP Id: rs1713611712

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149009686_149009687del , CM000665.2:g.149009686_149009687del GRCh38
NC_000003.11:g.148727473_148727474del , CM000665.1:g.148727473_148727474del GRCh37
NC_000003.10:g.150210163_150210164del NCBI36
NG_027677.1:g.23279_23280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000345003.9:c.608+284_608+285del MANE Select ENSP00000340736.4:n.608+284_608+285del
ENST00000296048.10:c.608+284_608+285del ENSP00000296048.6:n.608+284_608+285del
ENST00000345003.8:c.608+284_608+285del ENSP00000340736.4:n.608+284_608+285del
ENST00000461191.1:c.596+284_596+285del ENSP00000420247.1:n.596+284_596+285del
ENST00000469873.1:n.522+284_522+285del
ENST00000479119.1:n.224+284_224+285del
ENST00000483267.5:c.469+12794_469+12795del ENSP00000419499.1:n.469+12794_469+12795del
ENST00000484197.5:c.608+284_608+285del ENSP00000420683.1:n.608+284_608+285del
ENST00000627418.2:c.469+12794_469+12795del ENSP00000486061.1:n.469+12794_469+12795del
NM_001184720.1:c.608+284_608+285del NP_001171649.1:n.608+284_608+285del
NM_001184721.1:c.608+284_608+285del NP_001171650.1:n.608+284_608+285del
NM_004130.3:c.608+284_608+285del NP_004121.2:n.608+284_608+285del
XM_017006275.1:c.431+284_431+285del XP_016861764.1:n.431+284_431+285del
XM_017006276.1:c.146+284_146+285del XP_016861765.1:n.146+284_146+285del
NM_004130.4:c.608+284_608+285del MANE Select NP_004121.2:n.608+284_608+285del
NM_001184720.2:c.608+284_608+285del NP_001171649.1:n.608+284_608+285del
NM_001184721.2:c.608+284_608+285del NP_001171650.1:n.608+284_608+285del