Canonical Allele Identifier: CA14311040
Gene: CLEC16A HGNC NCBI

Linked Data

dbSNP Id: rs12599402

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11096031T>C , CM000678.2:g.11096031T>C GRCh38
NC_000016.9:g.11189888T>C , CM000678.1:g.11189888T>C GRCh37
NC_000016.8:g.11097389T>C NCBI36
NG_016757.1:g.156544T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000703130.1:c.2111-24584T>C ENSP00000515187.1:n.2111-24584T>C
ENST00000409790.6:c.2117-24584T>C MANE Select ENSP00000387122.1:n.2117-24584T>C
ENST00000646363.1:n.778-24584T>C
ENST00000409552.4:c.2063-24584T>C ENSP00000386495.3:n.2063-24584T>C
ENST00000409790.5:c.2117-24584T>C ENSP00000387122.1:n.2117-24584T>C
ENST00000465491.5:n.773-24584T>C
NM_001243403.1:c.2063-24584T>C NP_001230332.1:n.2063-24584T>C
NM_015226.2:c.2117-24584T>C NP_056041.1:n.2117-24584T>C
XM_005255210.1:c.2111-24584T>C XP_005255267.1:n.2111-24584T>C
XM_005255211.1:c.2069-24584T>C XP_005255268.1:n.2069-24584T>C
XM_005255213.1:c.2063-24584T>C XP_005255270.1:n.2063-24584T>C
XM_005255214.1:c.2117-24584T>C XP_005255271.1:n.2117-24584T>C
XM_005255215.3:c.2117-24584T>C XP_005255272.1:n.2117-24584T>C
XM_005255216.1:c.2117-24584T>C XP_005255273.1:n.2117-24584T>C
XM_011522434.1:c.1988-24584T>C XP_011520736.1:n.1988-24584T>C
XM_011522435.1:c.2117-24584T>C XP_011520737.1:n.2117-24584T>C
XM_011522436.1:c.2117-24584T>C XP_011520738.1:n.2117-24584T>C
XM_011522437.1:c.2117-24584T>C XP_011520739.1:n.2117-24584T>C
XM_011522438.1:c.2117-24584T>C XP_011520740.1:n.2117-24584T>C
XM_011522439.1:c.2117-24584T>C XP_011520741.1:n.2117-24584T>C
XM_011522440.1:c.2117-24584T>C XP_011520742.1:n.2117-24584T>C
XR_932810.1:n.2341-24584T>C
XM_005255210.2:c.2111-24584T>C XP_005255267.1:n.2111-24584T>C
XM_005255211.2:c.2069-24584T>C XP_005255268.1:n.2069-24584T>C
XM_005255213.2:c.2063-24584T>C XP_005255270.1:n.2063-24584T>C
XM_005255214.2:c.2117-24584T>C XP_005255271.1:n.2117-24584T>C
XM_005255215.4:c.2117-24584T>C XP_005255272.1:n.2117-24584T>C
XM_005255216.2:c.2117-24584T>C XP_005255273.1:n.2117-24584T>C
XM_011522434.2:c.1988-24584T>C XP_011520736.1:n.1988-24584T>C
XM_011522435.2:c.2117-24584T>C XP_011520737.1:n.2117-24584T>C
XM_011522436.3:c.2117-24584T>C XP_011520738.1:n.2117-24584T>C
XM_011522437.3:c.2117-24584T>C XP_011520739.1:n.2117-24584T>C
XM_011522438.3:c.2117-24584T>C XP_011520740.1:n.2117-24584T>C
XM_011522439.3:c.2117-24584T>C XP_011520741.1:n.2117-24584T>C
XM_011522440.3:c.2117-24584T>C XP_011520742.1:n.2117-24584T>C
XM_017023090.2:c.602-24584T>C XP_016878579.1:n.602-24584T>C
XM_024450218.1:c.2069-24584T>C XP_024305986.1:n.2069-24584T>C
XM_024450219.1:c.668-24584T>C XP_024305987.1:n.668-24584T>C
XR_932810.3:n.2296-24584T>C
NM_015226.3:c.2117-24584T>C MANE Select NP_056041.1:n.2117-24584T>C
NM_001243403.2:c.2063-24584T>C NP_001230332.1:n.2063-24584T>C