Canonical Allele Identifier: CA1410025478
Gene: GYG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148996137T= , CM000665.2:g.148996137T= GRCh38
NC_000003.11:g.148713924T= , CM000665.1:g.148713924T= GRCh37
NC_000003.10:g.150196614T= NCBI36
NG_027677.1:g.9730T=

Transcript Alleles

HGVS Amino-acid change
ENST00000345003.9:c.144-165T= MANE Select ENSP00000340736.4:n.144-165T=
ENST00000296048.10:c.144-165T= ENSP00000296048.6:n.144-165T=
ENST00000345003.8:c.144-165T= ENSP00000340736.4:n.144-165T=
ENST00000461191.1:c.144-165T= ENSP00000420247.1:n.144-165T=
ENST00000465547.1:n.50-178T=
ENST00000473005.1:c.6-165T= ENSP00000417671.1:n.6-165T=
ENST00000478067.1:n.245-165T=
ENST00000483267.5:c.144-165T= ENSP00000419499.1:n.144-165T=
ENST00000484197.5:c.144-165T= ENSP00000420683.1:n.144-165T=
ENST00000492285.6:c.6-165T= ENSP00000418297.2:n.6-165T=
ENST00000627418.2:c.144-165T= ENSP00000486061.1:n.144-165T=
NM_001184720.1:c.144-165T= NP_001171649.1:n.144-165T=
NM_001184721.1:c.144-165T= NP_001171650.1:n.144-165T=
NM_004130.3:c.144-165T= NP_004121.2:n.144-165T=
XM_017006275.1:c.-34-165T= XP_016861764.1:n.-34-165T=
NM_004130.4:c.144-165T= MANE Select NP_004121.2:n.144-165T=
NM_001184720.2:c.144-165T= NP_001171649.1:n.144-165T=
NM_001184721.2:c.144-165T= NP_001171650.1:n.144-165T=