Canonical Allele Identifier: CA2207456142
Gene: CLEC16A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11148060C= , CM000678.2:g.11148060C= GRCh38
NC_000016.9:g.11241917C= , CM000678.1:g.11241917C= GRCh37
NC_000016.8:g.11149418C= NCBI36
NG_016757.1:g.208573C=

Transcript Alleles

HGVS Amino-acid change
ENST00000703130.1:c.2636-18328C= ENSP00000515187.1:n.2636-18328C=
ENST00000409790.6:c.2642-18328C= MANE Select ENSP00000387122.1:n.2642-18328C=
ENST00000261657.5:c.216-18328C=
ENST00000409790.5:c.2642-18328C= ENSP00000387122.1:n.2642-18328C=
ENST00000428742.6:c.373-9017C=
ENST00000436973.5:c.221-8514C= ENSP00000389963.1:n.221-8514C=
ENST00000459723.1:n.138-1826C=
NM_015226.2:c.2642-18328C= NP_056041.1:n.2642-18328C=
XM_005255210.1:c.2636-18328C= XP_005255267.1:n.2636-18328C=
XM_005255211.1:c.2594-18328C= XP_005255268.1:n.2594-18328C=
XM_005255213.1:c.2588-18328C= XP_005255270.1:n.2588-18328C=
XM_005255214.1:c.2641+21914C= XP_005255271.1:n.2641+21914C=
XM_005255215.3:c.2642-8514C= XP_005255272.1:n.2642-8514C=
XM_005255216.1:c.2642-9017C= XP_005255273.1:n.2642-9017C=
XM_011522434.1:c.2513-18328C= XP_011520736.1:n.2513-18328C=
XM_011522435.1:c.2642-18328C= XP_011520737.1:n.2642-18328C=
XM_011522438.1:c.2642-1826C= XP_011520740.1:n.2642-1826C=
XR_932810.1:n.2866-18328C=
XM_005255210.2:c.2636-18328C= XP_005255267.1:n.2636-18328C=
XM_005255211.2:c.2594-18328C= XP_005255268.1:n.2594-18328C=
XM_005255213.2:c.2588-18328C= XP_005255270.1:n.2588-18328C=
XM_005255214.2:c.2641+21914C= XP_005255271.1:n.2641+21914C=
XM_005255215.4:c.2642-8514C= XP_005255272.1:n.2642-8514C=
XM_005255216.2:c.2642-9017C= XP_005255273.1:n.2642-9017C=
XM_011522434.2:c.2513-18328C= XP_011520736.1:n.2513-18328C=
XM_011522435.2:c.2642-18328C= XP_011520737.1:n.2642-18328C=
XM_011522438.3:c.2642-1826C= XP_011520740.1:n.2642-1826C=
XM_017023090.2:c.1127-18328C= XP_016878579.1:n.1127-18328C=
XM_024450218.1:c.2594-8514C= XP_024305986.1:n.2594-8514C=
XM_024450219.1:c.1193-18328C= XP_024305987.1:n.1193-18328C=
XR_932810.3:n.2821-18328C=
NM_015226.3:c.2642-18328C= MANE Select NP_056041.1:n.2642-18328C=