Canonical Allele Identifier: CA342514299

Gene: S100A13

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153618986G>A , CM000663.2:g.153618986G>A	GRCh38
NC_000001.10:g.153591462G>A , CM000663.1:g.153591462G>A	GRCh37
NC_000001.9:g.151858086G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440685.7:c.206C>T	ENSP00000392767.2:p.Ser69Leu
ENST00000476133.6:c.206C>T MANE Select	ENSP00000507299.1:p.Ser69Leu
ENST00000339556.8:c.206C>T	ENSP00000344822.3:p.Ser69Leu
ENST00000392622.3:c.206C>T	ENSP00000376398.1:p.Ser69Leu
ENST00000392623.5:c.206C>T	ENSP00000376399.1:p.Ser69Leu
ENST00000440685.6:c.206C>T	ENSP00000392767.2:p.Ser69Leu
ENST00000476133.5:n.511C>T
ENST00000491177.1:n.2006C>T
NM_001024210.1:c.206C>T	NP_001019381.1:p.Ser69Leu
NM_001024211.1:c.206C>T	NP_001019382.1:p.Ser69Leu
NM_001024212.1:c.206C>T	NP_001019383.1:p.Ser69Leu
NM_001024213.1:c.206C>T	NP_001019384.1:p.Ser69Leu
NM_005979.2:c.206C>T	NP_005970.1:p.Ser69Leu
XM_005245434.3:c.206C>T	XP_005245491.1:p.Ser69Leu
XM_011509862.1:c.206C>T	XP_011508164.1:p.Ser69Leu
XM_011509863.1:c.206C>T	XP_011508165.1:p.Ser69Leu
XM_011509864.1:c.206C>T	XP_011508166.1:p.Ser69Leu
XM_011509862.3:c.206C>T	XP_011508164.1:p.Ser69Leu
XM_011509863.3:c.206C>T	XP_011508165.1:p.Ser69Leu
XM_011509864.2:c.206C>T	XP_011508166.1:p.Ser69Leu
XM_017002034.2:c.206C>T	XP_016857523.1:p.Ser69Leu
XM_017002035.2:c.206C>T	XP_016857524.1:p.Ser69Leu
XM_017002036.1:c.206C>T	XP_016857525.1:p.Ser69Leu
NM_001024210.2:c.206C>T	NP_001019381.1:p.Ser69Leu
NM_001024211.2:c.206C>T MANE Select	NP_001019382.1:p.Ser69Leu
NM_001024212.2:c.206C>T	NP_001019383.1:p.Ser69Leu
NM_001024213.2:c.206C>T	NP_001019384.1:p.Ser69Leu
NM_005979.3:c.206C>T	NP_005970.1:p.Ser69Leu