Canonical Allele Identifier: CA341826703
Gene: SLC16A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.113456546A>C (hg19) chr1:g.112913924A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112913924A>C , CM000663.2:g.112913924A>C GRCh38
NC_000001.10:g.113456546A>C , CM000663.1:g.113456546A>C GRCh37
NC_000001.9:g.113258069A>C NCBI36
NG_015880.2:g.47005T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369626.8:c.1470T>G MANE Select ENSP00000358640.4:p.Asp490Glu
ENST00000429288.2:c.1470T>G ENSP00000397106.2:p.Asp490Glu
ENST00000443580.6:c.1470T>G ENSP00000399104.2:p.Asp490Glu
ENST00000458229.6:c.1470T>G ENSP00000416167.2:p.Asp490Glu
ENST00000679803.1:c.1470T>G ENSP00000505879.1:p.Asp490Glu
ENST00000369626.7:c.1470T>G ENSP00000358640.3:p.Asp490Glu
ENST00000538576.5:c.1470T>G ENSP00000441065.1:p.Asp490Glu
NM_001166496.1:c.1470T>G NP_001159968.1:p.Asp490Glu
NM_003051.3:c.1470T>G NP_003042.3:p.Asp490Glu
XM_011542026.1:c.1470T>G XP_011540328.1:p.Asp490Glu
XM_011542027.1:c.1470T>G XP_011540329.1:p.Asp490Glu
NM_003051.4:c.1470T>G MANE Select NP_003042.3:p.Asp490Glu
NM_001166496.2:c.1470T>G NP_001159968.1:p.Asp490Glu
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