Canonical Allele Identifier: CA1116787

Gene: S100A13

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153626370C>T , CM000663.2:g.153626370C>T	GRCh38
NC_000001.10:g.153598846C>T , CM000663.1:g.153598846C>T	GRCh37
NC_000001.9:g.151865470C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440685.7:c.103G>A	ENSP00000392767.2:p.Val35Ile
ENST00000476133.6:c.103G>A MANE Select	ENSP00000507299.1:p.Val35Ile
ENST00000339556.8:c.103G>A	ENSP00000344822.3:p.Val35Ile
ENST00000392622.3:c.103G>A	ENSP00000376398.1:p.Val35Ile
ENST00000392623.5:c.103G>A	ENSP00000376399.1:p.Val35Ile
ENST00000440685.6:c.103G>A	ENSP00000392767.2:p.Val35Ile
ENST00000476133.5:n.408G>A
ENST00000491177.1:n.1903G>A
NM_001024210.1:c.103G>A	NP_001019381.1:p.Val35Ile
NM_001024211.1:c.103G>A	NP_001019382.1:p.Val35Ile
NM_001024212.1:c.103G>A	NP_001019383.1:p.Val35Ile
NM_001024213.1:c.103G>A	NP_001019384.1:p.Val35Ile
NM_005979.2:c.103G>A	NP_005970.1:p.Val35Ile
XM_005245434.3:c.103G>A	XP_005245491.1:p.Val35Ile
XM_011509862.1:c.103G>A	XP_011508164.1:p.Val35Ile
XM_011509863.1:c.103G>A	XP_011508165.1:p.Val35Ile
XM_011509864.1:c.103G>A	XP_011508166.1:p.Val35Ile
XM_011509862.3:c.103G>A	XP_011508164.1:p.Val35Ile
XM_011509863.3:c.103G>A	XP_011508165.1:p.Val35Ile
XM_011509864.2:c.103G>A	XP_011508166.1:p.Val35Ile
XM_017002034.2:c.103G>A	XP_016857523.1:p.Val35Ile
XM_017002035.2:c.103G>A	XP_016857524.1:p.Val35Ile
XM_017002036.1:c.103G>A	XP_016857525.1:p.Val35Ile
NM_001024210.2:c.103G>A	NP_001019381.1:p.Val35Ile
NM_001024211.2:c.103G>A MANE Select	NP_001019382.1:p.Val35Ile
NM_001024212.2:c.103G>A	NP_001019383.1:p.Val35Ile
NM_001024213.2:c.103G>A	NP_001019384.1:p.Val35Ile
NM_005979.3:c.103G>A	NP_005970.1:p.Val35Ile