Canonical Allele Identifier: CA277756499

Gene: CLEC16A

Linked Data

• dbSNP Id: rs770648300
• MyVariant Identifiers: chr16:g.11241927C>T (hg19) ; chr16:g.11148070C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11148070C>T , CM000678.2:g.11148070C>T	GRCh38
NC_000016.9:g.11241927C>T , CM000678.1:g.11241927C>T	GRCh37
NC_000016.8:g.11149428C>T	NCBI36
NG_016757.1:g.208583C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703130.1:c.2636-18318C>T	ENSP00000515187.1:n.2636-18318C>T
ENST00000409790.6:c.2642-18318C>T MANE Select	ENSP00000387122.1:n.2642-18318C>T
ENST00000261657.5:c.216-18318C>T
ENST00000409790.5:c.2642-18318C>T	ENSP00000387122.1:n.2642-18318C>T
ENST00000428742.6:c.373-9007C>T
ENST00000436973.5:c.221-8504C>T	ENSP00000389963.1:n.221-8504C>T
ENST00000459723.1:n.138-1816C>T
NM_015226.2:c.2642-18318C>T	NP_056041.1:n.2642-18318C>T
XM_005255210.1:c.2636-18318C>T	XP_005255267.1:n.2636-18318C>T
XM_005255211.1:c.2594-18318C>T	XP_005255268.1:n.2594-18318C>T
XM_005255213.1:c.2588-18318C>T	XP_005255270.1:n.2588-18318C>T
XM_005255214.1:c.2641+21924C>T	XP_005255271.1:n.2641+21924C>T
XM_005255215.3:c.2642-8504C>T	XP_005255272.1:n.2642-8504C>T
XM_005255216.1:c.2642-9007C>T	XP_005255273.1:n.2642-9007C>T
XM_011522434.1:c.2513-18318C>T	XP_011520736.1:n.2513-18318C>T
XM_011522435.1:c.2642-18318C>T	XP_011520737.1:n.2642-18318C>T
XM_011522438.1:c.2642-1816C>T	XP_011520740.1:n.2642-1816C>T
XR_932810.1:n.2866-18318C>T
XM_005255210.2:c.2636-18318C>T	XP_005255267.1:n.2636-18318C>T
XM_005255211.2:c.2594-18318C>T	XP_005255268.1:n.2594-18318C>T
XM_005255213.2:c.2588-18318C>T	XP_005255270.1:n.2588-18318C>T
XM_005255214.2:c.2641+21924C>T	XP_005255271.1:n.2641+21924C>T
XM_005255215.4:c.2642-8504C>T	XP_005255272.1:n.2642-8504C>T
XM_005255216.2:c.2642-9007C>T	XP_005255273.1:n.2642-9007C>T
XM_011522434.2:c.2513-18318C>T	XP_011520736.1:n.2513-18318C>T
XM_011522435.2:c.2642-18318C>T	XP_011520737.1:n.2642-18318C>T
XM_011522438.3:c.2642-1816C>T	XP_011520740.1:n.2642-1816C>T
XM_017023090.2:c.1127-18318C>T	XP_016878579.1:n.1127-18318C>T
XM_024450218.1:c.2594-8504C>T	XP_024305986.1:n.2594-8504C>T
XM_024450219.1:c.1193-18318C>T	XP_024305987.1:n.1193-18318C>T
XR_932810.3:n.2821-18318C>T
NM_015226.3:c.2642-18318C>T MANE Select	NP_056041.1:n.2642-18318C>T