Canonical Allele Identifier: CA2207440829

Gene: CLEC16A

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11121178A>C , CM000678.2:g.11121178A>C	GRCh38
NC_000016.9:g.11215035A>C , CM000678.1:g.11215035A>C	GRCh37
NC_000016.8:g.11122536A>C	NCBI36
NG_016757.1:g.181691A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703130.1:c.2262+412A>C	ENSP00000515187.1:n.2262+412A>C
ENST00000409790.6:c.2268+412A>C MANE Select	ENSP00000387122.1:n.2268+412A>C
ENST00000646363.1:n.929+412A>C
ENST00000409552.4:c.2214+412A>C	ENSP00000386495.3:n.2214+412A>C
ENST00000409790.5:c.2268+412A>C	ENSP00000387122.1:n.2268+412A>C
ENST00000465491.5:n.924+412A>C
NM_001243403.1:c.2214+412A>C	NP_001230332.1:n.2214+412A>C
NM_015226.2:c.2268+412A>C	NP_056041.1:n.2268+412A>C
XM_005255210.1:c.2262+412A>C	XP_005255267.1:n.2262+412A>C
XM_005255211.1:c.2220+412A>C	XP_005255268.1:n.2220+412A>C
XM_005255213.1:c.2214+412A>C	XP_005255270.1:n.2214+412A>C
XM_005255214.1:c.2268+412A>C	XP_005255271.1:n.2268+412A>C
XM_005255215.3:c.2268+412A>C	XP_005255272.1:n.2268+412A>C
XM_005255216.1:c.2268+412A>C	XP_005255273.1:n.2268+412A>C
XM_011522434.1:c.2139+412A>C	XP_011520736.1:n.2139+412A>C
XM_011522435.1:c.2268+412A>C	XP_011520737.1:n.2268+412A>C
XM_011522436.1:c.2268+412A>C	XP_011520738.1:n.2268+412A>C
XM_011522437.1:c.2268+412A>C	XP_011520739.1:n.2268+412A>C
XM_011522438.1:c.2268+412A>C	XP_011520740.1:n.2268+412A>C
XM_011522439.1:c.2268+412A>C	XP_011520741.1:n.2268+412A>C
XM_011522440.1:c.2268+412A>C	XP_011520742.1:n.2268+412A>C
XR_932810.1:n.2492+412A>C
XM_005255210.2:c.2262+412A>C	XP_005255267.1:n.2262+412A>C
XM_005255211.2:c.2220+412A>C	XP_005255268.1:n.2220+412A>C
XM_005255213.2:c.2214+412A>C	XP_005255270.1:n.2214+412A>C
XM_005255214.2:c.2268+412A>C	XP_005255271.1:n.2268+412A>C
XM_005255215.4:c.2268+412A>C	XP_005255272.1:n.2268+412A>C
XM_005255216.2:c.2268+412A>C	XP_005255273.1:n.2268+412A>C
XM_011522434.2:c.2139+412A>C	XP_011520736.1:n.2139+412A>C
XM_011522435.2:c.2268+412A>C	XP_011520737.1:n.2268+412A>C
XM_011522436.3:c.2268+412A>C	XP_011520738.1:n.2268+412A>C
XM_011522437.3:c.2268+412A>C	XP_011520739.1:n.2268+412A>C
XM_011522438.3:c.2268+412A>C	XP_011520740.1:n.2268+412A>C
XM_011522439.3:c.2268+412A>C	XP_011520741.1:n.2268+412A>C
XM_011522440.3:c.2268+412A>C	XP_011520742.1:n.2268+412A>C
XM_017023090.2:c.753+412A>C	XP_016878579.1:n.753+412A>C
XM_024450218.1:c.2220+412A>C	XP_024305986.1:n.2220+412A>C
XM_024450219.1:c.819+412A>C	XP_024305987.1:n.819+412A>C
XR_932810.3:n.2447+412A>C
NM_015226.3:c.2268+412A>C MANE Select	NP_056041.1:n.2268+412A>C
NM_001243403.2:c.2214+412A>C	NP_001230332.1:n.2214+412A>C