Canonical Allele Identifier: CA436192393
Gene: GYG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.148714672T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148996885T>A , CM000665.2:g.148996885T>A GRCh38
NC_000003.11:g.148714672T>A , CM000665.1:g.148714672T>A GRCh37
NC_000003.10:g.150197362T>A NCBI36
NG_027677.1:g.10478T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000345003.9:c.462T>A MANE Select ENSP00000340736.4:p.Ser154=
ENST00000296048.10:c.462T>A ENSP00000296048.6:p.Ser154=
ENST00000345003.8:c.462T>A ENSP00000340736.4:p.Ser154=
ENST00000461191.1:c.462T>A ENSP00000420247.1:p.Ser154=
ENST00000483267.5:c.462T>A ENSP00000419499.1:p.Ser154=
ENST00000484197.5:c.462T>A ENSP00000420683.1:p.Ser154=
ENST00000492285.6:c.324T>A ENSP00000418297.2:p.Ser108=
ENST00000497528.5:n.55T>A
ENST00000627418.2:c.462T>A ENSP00000486061.1:p.Ser154=
NM_001184720.1:c.462T>A NP_001171649.1:p.Ser154=
NM_001184721.1:c.462T>A NP_001171650.1:p.Ser154=
NM_004130.3:c.462T>A NP_004121.2:p.Ser154=
XM_017006275.1:c.285T>A XP_016861764.1:p.Ser95=
NM_004130.4:c.462T>A MANE Select NP_004121.2:p.Ser154=
NM_001184720.2:c.462T>A NP_001171649.1:p.Ser154=
NM_001184721.2:c.462T>A NP_001171650.1:p.Ser154=