Canonical Allele Identifier: CA217091856

Gene: MMP26 OR51S1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.4848826A>G , CM000673.2:g.4848826A>G	GRCh38
NC_000011.9:g.4870056A>G , CM000673.1:g.4870056A>G	GRCh37
NC_000011.8:g.4826632A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001004758.1:c.383T>C (OR51S1) MANE Select	NP_001004758.1:p.Ile128Thr
NM_021801.5:c.-145+81485A>G (MMP26) MANE Select	NP_068573.2:n.-145+81485A>G
ENST00000322101.5:c.383T>C (OR51S1) MANE Select	ENSP00000322754.2:p.Ile128Thr
ENST00000380390.6:c.-145+81485A>G (MMP26) MANE Select	ENSP00000369753.1:n.-145+81485A>G
NM_001384608.1:c.-153+81485A>G (MMP26)	NP_001371537.1:n.-153+81485A>G
ENST00000300762.2:c.-153+81485A>G (MMP26)	ENSP00000300762.2:n.-153+81485A>G
ENST00000322101.3:c.383T>C (OR51S1)	ENSP00000322754.2:p.Ile128Thr
ENST00000322101.4:c.383T>C (OR51S1)	ENSP00000322754.2:p.Ile128Thr
ENST00000380390.5:c.-145+81485A>G (MMP26)	ENSP00000369753.1:n.-145+81485A>G
ENST00000477339.5:n.191+81485A>G (MMP26)
XM_011519884.1:c.383T>C (OR51S1)	XP_011518186.1:p.Ile128Thr