Canonical Allele Identifier: CA1116884

Gene: S100A1 S100A13

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153630640C>T , CM000663.2:g.153630640C>T	GRCh38
NC_000001.10:g.153603116C>T , CM000663.1:g.153603116C>T	GRCh37
NC_000001.9:g.151869740C>T	NCBI36
NG_030030.1:g.1659C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292169.6:c.119C>T (S100A1) MANE Select	ENSP00000292169.2:p.Thr40Met
ENST00000292169.5:c.119C>T (S100A1)	ENSP00000292169.1:p.Thr40Met
ENST00000368696.3:c.119C>T (S100A1)	ENSP00000357685.3:p.Thr40Met
ENST00000368698.3:c.278C>T (S100A1)	ENSP00000357687.3:p.Thr93Met
ENST00000469893.2:n.2257C>T (S100A1)
ENST00000491177.1:n.367G>A (S100A13)
NM_001024210.1:c.-62+371G>A (S100A13)	NP_001019381.1:n.-62+371G>A
NM_006271.1:c.119C>T (S100A1)	NP_006262.1:p.Thr40Met
XM_005245434.3:c.-295+371G>A (S100A13)	XP_005245491.1:n.-295+371G>A
XM_011509862.1:c.-295+371G>A (S100A13)	XP_011508164.1:n.-295+371G>A
XM_011509863.1:c.-295+371G>A (S100A13)	XP_011508165.1:n.-295+371G>A
XM_011509864.1:c.-485G>A (S100A13)	XP_011508166.1:n.-485G>A
XM_011509862.3:c.-295+371G>A (S100A13)	XP_011508164.1:n.-295+371G>A
XM_011509863.3:c.-295+371G>A (S100A13)	XP_011508165.1:n.-295+371G>A
XM_017002034.2:c.-178+371G>A (S100A13)	XP_016857523.1:n.-178+371G>A
XM_017002035.2:c.-179+371G>A (S100A13)	XP_016857524.1:n.-179+371G>A
NM_001024210.2:c.-62+371G>A (S100A13)	NP_001019381.1:n.-62+371G>A
NM_006271.2:c.119C>T (S100A1) MANE Select	NP_006262.1:p.Thr40Met