Canonical Allele Identifier: CA8335822
Community Standard Title: NM_001330070.2(CLEC10A):c.7A>G (p.Arg3Gly)
Gene: CLEC10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7078806T>C , CM000679.2:g.7078806T>C GRCh38
NC_000017.10:g.6982125T>C , CM000679.1:g.6982125T>C GRCh37
NC_000017.9:g.6922849T>C NCBI36
NG_029878.1:g.6476A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001330070.2:c.7A>G MANE Select NP_001316999.1:p.Arg3Gly
ENST00000416562.7:c.7A>G MANE Select ENSP00000414938.2:p.Arg3Gly
NM_001330070.1:c.7A>G NP_001316999.1:p.Arg3Gly
NM_006344.2:c.7A>G NP_006335.2:p.Arg3Gly
NM_006344.3:c.7A>G NP_006335.2:p.Arg3Gly
NM_006344.4:c.7A>G NP_006335.2:p.Arg3Gly
NM_182906.2:c.7A>G NP_878910.1:p.Arg3Gly
NM_182906.3:c.7A>G NP_878910.1:p.Arg3Gly
NM_182906.4:c.7A>G NP_878910.1:p.Arg3Gly
ENST00000254868.8:c.7A>G ENSP00000254868.4:p.Arg3Gly
ENST00000416562.6:c.7A>G ENSP00000414938.2:p.Arg3Gly
ENST00000571624.1:n.273A>G
ENST00000571664.1:c.7A>G ENSP00000460252.1:p.Arg3Gly
ENST00000576617.5:c.7A>G ENSP00000458728.1:p.Arg3Gly
XM_005256412.1:c.7A>G XP_005256469.1:p.Arg3Gly
XM_011523613.1:c.7A>G XP_011521915.1:p.Arg3Gly
XM_011523614.1:c.7A>G XP_011521916.1:p.Arg3Gly
XM_011523615.1:c.7A>G XP_011521917.1:p.Arg3Gly