Canonical Allele Identifier: CA2088224735
Gene: TSC22D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.44480912C= , CM000675.2:g.44480912C= GRCh38
NC_000013.10:g.45055048C= , CM000675.1:g.45055048C= GRCh37
NC_000013.9:g.43953048C= NCBI36
NG_029852.1:g.100654G=
NG_029852.2:g.100654G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000458659.3:c.2913-44817G= MANE Select ENSP00000397435.2:n.2913-44817G=
ENST00000458659.2:c.2913-44817G= ENSP00000397435.2:n.2913-44817G=
ENST00000501704.3:c.1664-46898G= ENSP00000437414.1:n.1664-46898G=
NM_001243799.1:c.1664-46898G= NP_001230728.1:n.1664-46898G=
NM_183422.3:c.2913-44817G= NP_904358.2:n.2913-44817G=
XM_024449427.1:c.2913-44817G= XP_024305195.1:n.2913-44817G=
NM_183422.4:c.2913-44817G= MANE Select NP_904358.2:n.2913-44817G=