Canonical Allele Identifier: CA2088224739
Gene: TSC22D1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.44480916T= , CM000675.2:g.44480916T= GRCh38
NC_000013.10:g.45055052T= , CM000675.1:g.45055052T= GRCh37
NC_000013.9:g.43953052T= NCBI36
NG_029852.1:g.100650A=
NG_029852.2:g.100650A=

Transcript Alleles

HGVS Amino-acid change
ENST00000458659.3:c.2913-44821A= MANE Select ENSP00000397435.2:n.2913-44821A=
ENST00000458659.2:c.2913-44821A= ENSP00000397435.2:n.2913-44821A=
ENST00000501704.3:c.1664-46902A= ENSP00000437414.1:n.1664-46902A=
NM_001243799.1:c.1664-46902A= NP_001230728.1:n.1664-46902A=
NM_183422.3:c.2913-44821A= NP_904358.2:n.2913-44821A=
XM_024449427.1:c.2913-44821A= XP_024305195.1:n.2913-44821A=
NM_183422.4:c.2913-44821A= MANE Select NP_904358.2:n.2913-44821A=
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