Canonical Allele Identifier: CA277720871

Gene: CLEC16A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11003622C>G , CM000678.2:g.11003622C>G	GRCh38
NC_000016.9:g.11097479C>G , CM000678.1:g.11097479C>G	GRCh37
NC_000016.8:g.11004980C>G	NCBI36
NG_016757.1:g.64135C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703130.1:c.1297+317C>G	ENSP00000515187.1:n.1297+317C>G
ENST00000409790.6:c.1303+317C>G MANE Select	ENSP00000387122.1:n.1303+317C>G
ENST00000409552.4:c.1249+365C>G	ENSP00000386495.3:n.1249+365C>G
ENST00000409790.5:c.1303+317C>G	ENSP00000387122.1:n.1303+317C>G
ENST00000494853.1:n.778+317C>G
NM_001243403.1:c.1249+365C>G	NP_001230332.1:n.1249+365C>G
NM_015226.2:c.1303+317C>G	NP_056041.1:n.1303+317C>G
XM_005255210.1:c.1297+317C>G	XP_005255267.1:n.1297+317C>G
XM_005255211.1:c.1255+365C>G	XP_005255268.1:n.1255+365C>G
XM_005255213.1:c.1249+365C>G	XP_005255270.1:n.1249+365C>G
XM_005255214.1:c.1303+317C>G	XP_005255271.1:n.1303+317C>G
XM_005255215.3:c.1303+317C>G	XP_005255272.1:n.1303+317C>G
XM_005255216.1:c.1303+317C>G	XP_005255273.1:n.1303+317C>G
XM_006720870.2:c.1303+317C>G	XP_006720933.1:n.1303+317C>G
XM_011522434.1:c.1303+317C>G	XP_011520736.1:n.1303+317C>G
XM_011522435.1:c.1303+317C>G	XP_011520737.1:n.1303+317C>G
XM_011522436.1:c.1303+317C>G	XP_011520738.1:n.1303+317C>G
XM_011522437.1:c.1303+317C>G	XP_011520739.1:n.1303+317C>G
XM_011522438.1:c.1303+317C>G	XP_011520740.1:n.1303+317C>G
XM_011522439.1:c.1303+317C>G	XP_011520741.1:n.1303+317C>G
XM_011522440.1:c.1303+317C>G	XP_011520742.1:n.1303+317C>G
XR_932810.1:n.1527+317C>G
XM_005255210.2:c.1297+317C>G	XP_005255267.1:n.1297+317C>G
XM_005255211.2:c.1255+365C>G	XP_005255268.1:n.1255+365C>G
XM_005255213.2:c.1249+365C>G	XP_005255270.1:n.1249+365C>G
XM_005255214.2:c.1303+317C>G	XP_005255271.1:n.1303+317C>G
XM_005255215.4:c.1303+317C>G	XP_005255272.1:n.1303+317C>G
XM_005255216.2:c.1303+317C>G	XP_005255273.1:n.1303+317C>G
XM_006720870.4:c.1303+317C>G	XP_006720933.1:n.1303+317C>G
XM_011522434.2:c.1303+317C>G	XP_011520736.1:n.1303+317C>G
XM_011522435.2:c.1303+317C>G	XP_011520737.1:n.1303+317C>G
XM_011522436.3:c.1303+317C>G	XP_011520738.1:n.1303+317C>G
XM_011522437.3:c.1303+317C>G	XP_011520739.1:n.1303+317C>G
XM_011522438.3:c.1303+317C>G	XP_011520740.1:n.1303+317C>G
XM_011522439.3:c.1303+317C>G	XP_011520741.1:n.1303+317C>G
XM_011522440.3:c.1303+317C>G	XP_011520742.1:n.1303+317C>G
XM_017023089.2:c.1249+365C>G	XP_016878578.1:n.1249+365C>G
XM_024450218.1:c.1255+365C>G	XP_024305986.1:n.1255+365C>G
XR_932810.3:n.1482+317C>G
NM_015226.3:c.1303+317C>G MANE Select	NP_056041.1:n.1303+317C>G
NM_001243403.2:c.1249+365C>G	NP_001230332.1:n.1249+365C>G