Canonical Allele Identifier: CA10781218

Gene: S100A8

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153390629T>C , CM000663.2:g.153390629T>C	GRCh38
NC_000001.10:g.153363105T>C , CM000663.1:g.153363105T>C	GRCh37
NC_000001.9:g.151629729T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368733.4:c.-22-72A>G MANE Select	ENSP00000357722.3:n.-22-72A>G
ENST00000368732.5:c.-22-72A>G	ENSP00000357721.1:n.-22-72A>G
ENST00000368733.3:c.-22-72A>G	ENSP00000357722.3:n.-22-72A>G
ENST00000477801.1:n.443A>G
NM_002964.4:c.-22-72A>G	NP_002955.2:n.-22-72A>G
XM_011509861.1:c.3-72A>G	XP_011508163.1:n.3-72A>G
NM_001319196.1:c.34-55A>G	NP_001306125.1:n.34-55A>G
NM_001319197.1:c.34-58A>G	NP_001306126.1:n.34-58A>G
NM_001319198.1:c.3-72A>G	NP_001306127.1:n.3-72A>G
NM_001319201.1:c.-22-72A>G	NP_001306130.1:n.-22-72A>G
NM_002964.5:c.-22-72A>G MANE Select	NP_002955.2:n.-22-72A>G
NM_001319198.2:c.3-72A>G	NP_001306127.1:n.3-72A>G
NM_001319201.2:c.-22-72A>G	NP_001306130.1:n.-22-72A>G