Canonical Allele Identifier: CA620810856

Gene: CLEC16A

Linked Data

• dbSNP Id: rs965316389
• gnomAD v2: 16-11228715-C-G
• gnomAD v3: 16-11134858-C-G
• gnomAD v4: 16-11134858-C-G
• MyVariant Identifiers: chr16:g.11228715C>G (hg19) ; chr16:g.11134858C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11134858C>G , CM000678.2:g.11134858C>G	GRCh38
NC_000016.9:g.11228715C>G , CM000678.1:g.11228715C>G	GRCh37
NC_000016.8:g.11136216C>G	NCBI36
NG_016757.1:g.195371C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703130.1:c.2635+8712C>G	ENSP00000515187.1:n.2635+8712C>G
ENST00000409790.6:c.2641+8712C>G MANE Select	ENSP00000387122.1:n.2641+8712C>G
ENST00000646363.1:n.1303-1211C>G
ENST00000261657.5:c.215+8712C>G
ENST00000409790.5:c.2641+8712C>G	ENSP00000387122.1:n.2641+8712C>G
ENST00000428742.6:c.372+8712C>G
ENST00000436973.5:c.220+8712C>G	ENSP00000389963.1:n.220+8712C>G
ENST00000459723.1:n.137+8712C>G
NM_015226.2:c.2641+8712C>G	NP_056041.1:n.2641+8712C>G
XM_005255210.1:c.2635+8712C>G	XP_005255267.1:n.2635+8712C>G
XM_005255211.1:c.2593+8712C>G	XP_005255268.1:n.2593+8712C>G
XM_005255213.1:c.2587+8712C>G	XP_005255270.1:n.2587+8712C>G
XM_005255214.1:c.2641+8712C>G	XP_005255271.1:n.2641+8712C>G
XM_005255215.3:c.2641+8712C>G	XP_005255272.1:n.2641+8712C>G
XM_005255216.1:c.2641+8712C>G	XP_005255273.1:n.2641+8712C>G
XM_011522434.1:c.2512+8712C>G	XP_011520736.1:n.2512+8712C>G
XM_011522435.1:c.2641+8712C>G	XP_011520737.1:n.2641+8712C>G
XM_011522436.1:c.2642-401C>G	XP_011520738.1:n.2642-401C>G
XM_011522437.1:c.2642-401C>G	XP_011520739.1:n.2642-401C>G
XM_011522438.1:c.2641+8712C>G	XP_011520740.1:n.2641+8712C>G
XM_011522439.1:c.2642-1211C>G	XP_011520741.1:n.2642-1211C>G
XM_011522440.1:c.2642-1214C>G	XP_011520742.1:n.2642-1214C>G
XR_932810.1:n.2865+8712C>G
XM_005255210.2:c.2635+8712C>G	XP_005255267.1:n.2635+8712C>G
XM_005255211.2:c.2593+8712C>G	XP_005255268.1:n.2593+8712C>G
XM_005255213.2:c.2587+8712C>G	XP_005255270.1:n.2587+8712C>G
XM_005255214.2:c.2641+8712C>G	XP_005255271.1:n.2641+8712C>G
XM_005255215.4:c.2641+8712C>G	XP_005255272.1:n.2641+8712C>G
XM_005255216.2:c.2641+8712C>G	XP_005255273.1:n.2641+8712C>G
XM_011522434.2:c.2512+8712C>G	XP_011520736.1:n.2512+8712C>G
XM_011522435.2:c.2641+8712C>G	XP_011520737.1:n.2641+8712C>G
XM_011522436.3:c.2642-401C>G	XP_011520738.1:n.2642-401C>G
XM_011522437.3:c.2642-401C>G	XP_011520739.1:n.2642-401C>G
XM_011522438.3:c.2641+8712C>G	XP_011520740.1:n.2641+8712C>G
XM_011522439.3:c.2642-1211C>G	XP_011520741.1:n.2642-1211C>G
XM_011522440.3:c.2642-1214C>G	XP_011520742.1:n.2642-1214C>G
XM_017023090.2:c.1126+8712C>G	XP_016878579.1:n.1126+8712C>G
XM_024450218.1:c.2593+8712C>G	XP_024305986.1:n.2593+8712C>G
XM_024450219.1:c.1192+8712C>G	XP_024305987.1:n.1192+8712C>G
XR_001752081.1:n.284+105G>C
XR_932810.3:n.2820+8712C>G
NM_015226.3:c.2641+8712C>G MANE Select	NP_056041.1:n.2641+8712C>G